Combinations and compositions which interfere with VEGF/ VEGF and angiopoietin/ Tie receptor function and their use (II)

ABSTRACT

The present invention describes the combination of substances interfering with the biological activity of Vascular Endothelial Growth Factor (VEGF)/VEGF receptor systems (compound I) and substances interfering with the biological function of Angiopoietin/Tie receptor systems (compound II) for inhibition of vascularization and for cancer treatment.

[0001] The present invention provides the combination of substances interfering with the biological activity of Vascular Endothelial Growth Factor (VEGF)/VEGF receptor systems (compound I) and substances interfering with the biological function of Angiopoietin/Tie receptor systems (compound II) for inhibition of vascularization and for cancer treatment.

[0002] Protein ligands and receptor tyrosine kinases that specifically regulate endothelial cell function are substantially involved in physiological as well as in disease-related angiogenesis. These ligand/receptor systems include the Vascular Endothelial Growth Factor (VEGF) and the Angiopoietin (Ang) families, and their receptors, the VEGF receptor family and the tyrosine kinase with immunoglobulin-like and epidermal growth factor homology domains (Tie) family. The members of the two families of receptor tyrosine kinases are expressed primarily on endothelial cells. The VEGF receptor family includes Flt1 (VEGF-R1), Flk1/KDR (VEGF-R2), and Flt4 (VEGF-R3). These receptors are recognized by members of the VEGF-related growth factors in that the ligands of Flt1 are VEGF and placenta growth factor (PIGF), whereas Flk1/KDR binds VEGF, VEGF-C and VEGF-D, and the ligands of Flt4 are VEGF-C and VEGF-D (Nicosia, Am. J. Pathol. 153, 11-16, 1998). The second family of endothelial cell specific receptor tyrosine kinases is represented by Tie1 and Tie2 (also kown as Tek). Whereas Tie1 remains an orphan receptor, three secreted glycoprotein ligands of Tie2, Ang1, Ang2, and Ang3/Ang4 have been discovered (Davis et al., Cell 87, 1161-1169, 1996; Maisonpierre et al., Science 277, 55-60, 1997; Valenzuela et al, Proc. Natl. Acad. Sci. USA 96, 1904-1909, 1999; patents: U.S. Pat. No. 5,521,073; U.S. Pat. No. 5,650,490; U.S. Pat. No. 5,814,464).

[0003] The pivotal role of VEGF and of its receptors during vascular development was exemplified in studies on targeted gene inactivation. Even the heterozygous disruption of the VEGF gene resulted in fatal deficiencies in vascularization (Carmeliet et al., Nature 380, 435-439, 1996; Ferrara et al., Nature 380, 439-442, 1996). Mice carrying homozygous disruptions in either Flt1 or Flk1/KDR gene die in mid-gestation of acute vascular defects. However, the phenotypes are distinct in that Flk1/KDR knock-out mice lack both endothelial cells and a developing hematopoietic system (Shalaby et al. Nature 376, 62-66, 1995), whereas Flt1 deficient mice have normal hematopoietic progenitors and endothelial cells, which fail to assemble into functional vessels (Fong et al., 376, 66-70, 1995). Disruption of the Flt4 gene, whose extensive embryonic expression becomes restricted to lymphatic vessels in adults, revealed an essential role of Flt4 for the remodeling and maturation of the primary vascular networks into larger blood vessels during early development of the cardiovascular system (Dumont et al., Science 282, 946-949, 1998). Consistent with the lymphatic expression of Flt4 in adults overexpression of VEGF-C in the skin of transgenic mice resulted in lymphatic, but not vascular, endothelial proliferation and vessel enlargement (Jeltsch et al., Science 276, 1423-1425, 1997). Moreover, VEGF-C was reported to induce neovascularization in mouse cornea and chicken embryo chorioallantoic membrane models of angiogenesis (Cao et al., Proc. Natl. Acad. Sci. USA 95, 14389-14394, 1998).

[0004] The second class of endothelial cell specific receptor tyrosine kinases has also been found to be critically involved in the formation and integrity of vasculature. Mice deficient in Tie1 die of edema and hemorrhage resulting from poor structural integrity of endothelial cells of the microvasculature (Sato et al., Nature 376, 70-74, 1995; Rodewald & Sato, Oncogene 12, 397-404, 1996). The Tie2 knock-out phenotype is characterized by immature vessels lacking branching networks and lacking periendothelial support cells (Sato et al., Nature 376, 70-74, 1995; Dumont et al., Genes Dev. 8, 1897-1909, 1994). Targeted inactivation of the Tie2 ligand Ang1, as well as overexpression of Ang2, an inhibitory ligand, resulted in phenotypes similar to the Tie2 knock out (Maisonpierre et al., Science 277, 55-60, 1997; Suri et al., cell 87, 1171-1180). Conversely, increased vascularization was observed upon transgenic overexpression of Ang1 (Suri et al., Science 282, 468-471, 1998; Thurstonen et al., Science 286, 2511-2514, 1999).

[0005] The results from angiogenic growth factor expression studies in corpus luteum development (Maisonpierre et al., Science 277, 55-60, 1997; Goede et al. Lab. Invest. 78, 1385-1394, 1998), studies on blood vessel maturation in the retina (Alon et al., Nature Med. 1, 1024-1028, 1995; Benjamin et al, Development 125, 1591-1598, 1998), and gene targeting and transgenic experiments on Tie2, Ang1, and Ang2, suggest a fundamental role of the Angiopoietin/Tie receptor system in mediating interactions between endothelial cells and surrounding pericytes or smooth muscle cells. Ang1, which is expressed by the periendothelial cells and seems to be expressed constitutively in the adult, is thought to stabilize existing mature vessels. Ang2, the natural antagonist of Ang1 which is expressed by endothelial cells at sites of vessel sprouting, seems to mediate loosening of endothelial-periendothelial cell contacts to allow vascular remodeling and sprouting in cooperation With angiogenesis initiators such as VEGF, or vessel regression in the absence of VEGF (Hanahan, Science 277, 48-50, 1997).

[0006] In pathological settings associated with aberrant neovascularization elevated expression of angiogenic growth factors and of their receptors has been observed. Most solid tumors express high levels of VEGF and the VEGF receptors appear predominantly in endothelial cells of vessels surrounding or penetrating the malignant tissue (Plate et al., Cancer Res. 53, 5822-5827, 1993). Interference with the VEGF/VEGF receptor system by means of VEGF-neutralizing antibodies (Kim et al., Nature 362, 841-844, 1993), retroviral expression of dominant negative VEGF receptor variants (Millauer et al., Nature 367, 576-579, 1994), recombinant VEGF-neutralizing receptor variants (Goldman et al., Proc. Natl. Acad. Sci. USA 95, 8795-8800, 1998), or small molecule inhibitors of VEGF receptor tyrosine kinase (Fong et al., Cancer Res. 59, 99-106, 1999; Wedge et al., Cancer Res. 60, 970-975, 2000; Wood et al. Cancer Res. 60, 2178-2189, 2000), or targeting cytotoxic agents via the VEGF/VEGF receptor system (Arora et al., Cancer Res. 59, 183-188, 1999; EP 0696456A2) resulted in reduced tumor growth and tumor vascularization. However, although many tumors were inhibited by interference with the VEGF/VEGF receptor system, others were unaffected (Millauer et al., Cancer Res. 56, 1615-1620, 1996). Human tumors as well as experimental tumor xenografts contain a large number of immature blood vessels that have not yet recruited periendothelial cells. The fraction of immature vessels is in the range of 40% in slow growing prostate cancer and 90% in fast growing glioblastoma. A selective obliteration of immature tumor vessels was observed upon withdrawal of VEGF by means of downregulation of VEGF transgene expression in a C6 glioblastoma xenograft model. This result is in accordance with a function of VEGF as endothelial cell survival factor. Similarly, in human prostate cancer shutting off VEGF expression as a consequence of androgen-ablation therapy led to selective apoptotic death of endothelial cells in vessels lacking periendothelial cell coverage. In contrast, the fraction of vessels which resisted VEGF withdrawal showed periendothelial cell coverage (Benjamin et al., J. Clin. Invest. 103, 159-165, 1999).

[0007] The observation of elevated expression of Tie receptors in the endothelium of metastatic melanomas (Kaipainen et al., Cancer Res. 54, 6571-6577, 1994), in breast carcinomas (Salven et al., Br. J. Cancer 74, 69-72, 1996), and in tumor xenografts grown in the presence of dominant-negative VEGF receptors (Millauer et al., Cancer Res. 56, 1615-1620, 1996), as well as elevated expression of Flt4 receptors in the endothelium of lymphatic vessels surrounding lymphomas and breast carcinomas (Jussila et al., Cancer Res. 58, 1599-1604, 1998), and of VEGF-C in various human tumor samples (Salvén et al., Am. J. Pathol. 153, 103-108, 1998), suggested these endothelium-specific growth factors and receptors as candidate alternative pathways driving tumor neovascularization. The high upregulation of Ang2 expression already in early tumors has been interpreted in terms of a host defense mechanism against initial cooption of existing blood vessels by the developing tumor. In the absence of VEGF, the coopted vessels undergo regression leading to necrosis within the center of the tumor. Contrarily, hypoxic upregulation of VEGF expression in cooperation with elevated Ang2 expression rescues and supports tumor vascularization and tumor growth at the tumor margin (Holash et al., Science 284, 1994-1998, 1999; Holash et al., Oncogene 18, 5356-5362, 1999).

[0008] Interference with Tie2 receptor function by means of Angiopoietin-neutralizing Tie2 variants consisting of the extracellular ligand-binding domain has been shown to result in inhibition of growth and vascularization of experimental tumors (Lin et al., J. Clin. Invest. 103, 159-165, 1999; Lin et al. Proc. Natl. Acad. Sci. USA 95, 8829-8834, 1998; Siemeister et al., Cancer Res. 59, 3185-3191, 1999). Comparing the effects of interference with the endothelium-specific receptor tyrosine kinase pathways by means of paracrine expression of the respective extracellular receptor domains on the same cellular background demonstrated inhibition of tumor growth upon blockade of the VEGF receptor system and of the Tie2 receptor system, respectively (Siemeister et al., Cancer Res. 59, 3185-3191, 1999).

[0009] It is known that the inhibition of the VEGF/VEGR receptor system by various methods resulted only in slowing down growth of most experimental tumors (Millauer et al., Nature 367, 576-579, 1994; Kim et al., Nature 362, 841-844, 1993; Millauer et al., Cancer Res. 56, 1615-1620, 1996; Goldman et al., Proc. Natl. Acad. Sci. USA 95, 8795-8800, 1998; Fong et al., Cancer Res. 59, 99-106, 1999; Wedge et al., Cancer Res. 60, 970-975, 2000; Wood et al. Cancer Res. 60, 2178-2189, 2000; Siemeister et al., Cancer Res. 59, 3185-3191, 1999). Even by escalation of therapeutic doses a plateau level of therapeutic efficacy was achieved (Kim et al., Nature 362, 841-844, 1993; Wood et al. Cancer Res. 60, 2178-2189, 2000). Similar results were observed upon interference with the Angiopoietin/Tie2 receptor system (Lin et al., J. Clin. Invest. 103, 159-165, 1999; Lin et al., Proc. Natl. Acad. Sci. USA 95, 8829-8834, 1998; Siemeister et al., Cancer Res. 59, 3185-3191, 1999).

[0010] However, there is a high demand for methods that enhance the therapeutic efficacy of anti-angiogenous compounds.

[0011] Searching for methods that enhance the therapeutic efficacy of anti-angiogenic compounds, superior anti-tumor effects were observed unexpectedly upon combination of inhibition of VEGF/VEGF receptor systems and interference with biological function of Angiopoietin/Tie receptor systems. The mode of action underlying the superior effects observed may be that interference biological function of Angiopoietin/Tie receptor systems destabilizes endothelial cell-periendothelial cell interaction of existing mature tumor vessels and thereby sensitizes the endothelium to compounds directed against VEGF/VEGF receptor systems.

[0012] Based on this unexpected finding the present invention provides the combination of functional interference with VEGF/VEGF receptor systems and with Angiopoietin/Tie receptor systems for inhibition of vascularization and of tumor growth.

[0013] The pharmaceutical composition consists of two components: compound I inhibits the biological activity of one or several of the VEGF/VEGF receptor systems or consists of cytotoxic agents which are targeted to the endothelium via recognition of VEGF/VEGF receptor systems. Compound II interferes with the biological function of one or several of Angiopoietin/Tie receptor systems or consists of cytotoxic agents which are targeted to the endothelium via recognition of Angiopoietin/Tie receptor systems. Alternatively, compound I inhibits the biological activity of one or several of the VEGF/VEGF receptor systems or of the Angiopoietin/Tie receptor systems and coumpound II consists of cytotoxic agents which are targeted to the endothelium via recognition of one or several of the VEGF/VEGF receptor systems or of the Angiopoietin/Tie receptor systems. Targeting or modulation of the biological activities of VEGF/VEGF receptor systems and of Angiopietin/Tie receptor systems can be performed by

[0014] (a) compounds which inhibit receptor tyrosine kinase activity,

[0015] (b) compounds which inhibit ligand binding to receptors,

[0016] (c) compounds which inhibit activation of intracellular signal pathways of the receptors,

[0017] (d) compounds which inhibit or activate expression of a ligand or of a receptor of the VEGF or Tie receptor system,

[0018] (e) delivery systems, such as antibodies, ligands, high-affinity binding oligonucleotides or oligopeptides, or liposomes, which target oytotoxic agents or coagulation-inducing agents to the endothelium via recognition of VEGF/VEGF receptor or Angiopoietin/Tie receptor systems,

[0019] (f) delivery systems, such as antibodies, ligands, high-affinity binding oligonucleotides or oligopeptides, or liposomes, which are targeted to the endothelium and induce necrosis or apoptosis.

[0020] A compound comprised by compositions of the present invention can be a small molecular weight substance, an oligonucleotide, an oligopeptide, a recombinant protein, an antibody, or conjugates or fusionproteins thereof. An example of an inhibitor is a small molecular weight molecule which inactivates a receptor tyrosine kinase by binding to and occupying the catalytic site such that the biological activity of the receptor is decreased. Kinase inhibitors are known in the art (Sugen: SU5416, SU6668; Fong et al. (1999), Cancer Res. 59, 99-106; Vajkoczy et al., Proc. Am. Associ. Cancer Res. San Francisco (2000), Abstract ID 3612; Zeneca: ZD4190, ZD6474; Wedge et al. (2000), Cancer Res. 60, 970-975; Parke-Davis PD0173073, PD0173074; Johnson et al., Proc. Am. Associ. Cancer Res., San Franzisco (2000), Abstract ID 3614; Dimitroff et al. (1999), Invest. New Drugs 17, 121-135). An example of an antagonist is a recombinant protein or an antibody which binds to a ligand such that activation of the receptor by the ligand is prevented. Another example of an antagonist is an antibody which binds to the receptor such that activation of the receptor is prevented. An example of an expression modulator is an antisense RNA or ribozyme which controls expression of a ligand or a receptor. An example of a targeted cytotoxic agent is a fusion protein of a ligand with a bacterial or plant toxin such as Pseudomonas exotoxin A, Diphtheria toxin, or Ricin A. An example of a targeted coagulation-inducing agent is a conjugate of a single chain antibody and tissue factor. Ligand-binding inhibitors such as neutralizing antibodies which are known in the art are described by Genentech (rhuMAbVEGF) and by Presta et al. (1997), Cancer Res. 57, 4593-4599. Ligand-binding receptor domaines are described by Kendall & Thomas (1993), Proc. Natl. Acad. Sci., U.S.A.90, 10705-10709; by Goldman et al. (1998) Proc. Natl. Acad. Sci., U.S.A.95, 8795-8800 and by Lin et al. (1997), J. Clin. Invest. 100, 2072-2078. Further, dominant negative receptors have been described by Millauer et al. (1994), Nature 367, 567-579.

[0021] Receptor blocking antibodies have been described by Imclone (cp1C11, U.S. Pat. No. 5,874,542). Further known are antagonistic ligand mutants (Siemeister et al. (1998), Proc. Natl. Acad. Sci., U.S.A.95, 4625-4629). High affinity ligand- or receptor binding oligo nucleotides habe been described by NeXstar (NX-244) and Drolet et al. (1996), Nat. Biotech 14, 1021-1025. Further, small molecules and peptides have been described.

[0022] Expression regulators have been described as anti-sense oligo nucleotides and as ribozymes-(RPI, Angiozyme™, see RPI Homepage).

[0023] Examples for delivery-/Targeting-Systems have been described as ligand/antibody-toxin-fusion-proteins or conjugates (Arora et al. (1999), Cancer Res. 59, 183-188 and Olson et al. (1997), Int. J. Cancer 73, 865-870), as endothel cell targeting of liposomes (Spragg et al. (1997), Prog. Natl. Acad. Sci, U.S.A94, 8795-8800, and as endothel cell targeting plus coagulation-induction (Ran et al., (1998), Cancer Res. 58, 4646-4653).

[0024] Small molecules which inhibit the receptor tyrosine kinase activity are for example molecules of general formula I

[0025] in which

[0026] r has the meaning of 0 to 2,

[0027] n has the meaning of 0 to 2;

[0028] R₃ und R₄ a) each independently from each other have the meaning of lower alkyl,

[0029] b) together form a bridge of general partial formula II,

[0030] wherein the binding is via the two terminal C-atoms, and

[0031] m has the meaning of 0 to 4; or

[0032] c) together form a bridge of partial formula III

[0033] wherein one or two of the ring members T₁,T₂,T₃ ,T₄ has the meaning of nitrogen, and each others have the meaning of CH, and the bining is via the atoms T₁ and T₄;

[0034] G has the meaning of C₁-C₆-alkyl, C₂-C₆-alkylene or C₂-C₆-alkenylene; or C₂-C₆-alkylene or C₃-C₆-alkenylene, which are substituted with acyloxy or hydroxy; —CH₂—O—, —CH₂—S—, —CH₂—NH—, —CH₂—O—CH₂—, —CH₂—S—CH₂—, —CH₂—NH—CH₂, oxa (—O—), thia (—S—) or imino (—NH—),

[0035] A, B, D, E and T independently from each other have the meaning of N or CH, with the provisio that not more than three of these Substituents have the meaning of N,

[0036] Q has the meaning of lower alkyl, lower alkyloxy or halogene,

[0037] R₁ and R₂ independently from each other have the meaning of H or lower alkyl,

[0038] X has the meaning of imino, oxa or thia;

[0039] Y has the meaning of hydrogene, unsubstituted or substituted aryl, heteroaryl, or unsubstituted or substituted cycloalkyl; and

[0040] Z has the meaning of amino, mono- or disubstituted amino, halogen, alkyl, substituted alkyl, hydroxy, etherificated or esterificated hydroxy, nitro, cyano, carboxy, esterificated carboxy, alkanoyl, carbamoyl, N-mono- or N,N-disubstituted carbamoyl, amidino, guanidino, mercapto, sulfo, phenylthio, phenyl-lower-alkyl-thio, alkyl-phenyl-thio, phenylsulfinyl, phenyl-lower-alkyl-sulfinyl, alkylphenylsulfinyl, phenylsulfonyl, phenyl-lower-alkan-sulfonyl, or alkylphenylsulfonyl, whereas, if more than one rest Z is present (m≧2), the substituents Z are equal or different from each other, and wherein the bonds marked with an arrow are single or double bonds; or an N-oxide of said compound, wherein one ore more N-atoms carry an oxygene atom, or a salt thereof.

[0041] A preferred salt is the salt of an organic acid, especially a succinate.

[0042] These compounds can preferentially be used as compound I or II in the inventive pharmaceutical composition.

[0043] Compounds which stop a tyrosin phosphorylation, or the persistent angiogenese, respectively, which results in a prevention of tumor growth and tumor spread, are for example

[0044] anthranyl acid derivatives of general formula IV

[0045] in which

[0046] A has the meaning of group ═NR²,

[0047] W has the meaning of oxygen, sulfur, two hydrogen atoms or the group ═NR⁸,

[0048] Z has the meaning of the group ═NR¹⁰ or ═N—, —N(R¹⁰)—(CH₂)_(q)-, branched or unbranched C₁₋₆-Alkyl or is the group

[0049] or A, Z and R¹ together form the group

[0050] m, n and o has the meaning of 0-3,

[0051] q has the meaning of 1-6,

[0052] R_(a), R_(b), R_(c), R_(d), R_(e), R_(f) independently from each other have the meaning of hydrogen, C₁₋₄ alkyl or the group ═NR¹⁰, and/or R_(a) and/or R_(b) together with R_(c) and or R_(d) or R_(c) together with R_(e) and/or R_(f) form a bound, or up to two of the groups R_(a)-R_(f) form a bridge with each up to 3 C-atoms with R¹ or R²,

[0053] X has the meaning of group ═NR⁹ or ═N—,

[0054] Y has the meaning of group —(CH₂)_(p),

[0055] p has the meaning of integer 14,

[0056] R¹ has the meaning of unsubstituted or optionally substituted with one or more of halogene, C₁₋₆-alkyl, or C₁₋₆-alkyl or C₁₋₆-alkoxy, which is optionally substituted by one or more of halogen, or is unsubstituted or substituted aryl or heteroaryl,

[0057] R² has the meaning of hydrogen or C₁₋₆-alkyl, or form a bridge with up to 3 ring atoms with R_(a)-R_(f) together with Z or R₁,

[0058] R³ has the meaning of monocyclic or bicyclic aryl or heteroaryl which is unsubstituted or optionally substituted with one or more of fur halogen, C₁₋₆-alkyl, C₁₋₆-alkoxy or hydroxy,

[0059] R⁴ ,R⁵, R⁶ and R⁷ independently from each other have the meaning of hydrogen, halogen or C₁₋₆-alkoxy, C₁₋₆-alkyl or C₁₋₆-carboxyalkyl, which are unsubstituted or optionally substituted with one or more of halogen, or R⁵ and R⁶ together form the group

[0060] R⁸, R⁹ and R¹⁰ independently from each other have the meaning of hydrogen or C₁₋₆-alkyl, as well as their isomers and salts.

[0061] These compounds can also preferentially be used as compound I or II in the inventive pharmaceutical composition.

[0062] More preferentially compounds of genearal formula V

[0063] in which

[0064] R¹ has the meaning of group

[0065] in which R⁵ is chloro, bromo or the group —OCH₃,

[0066] in which R⁷ is —CH₃ or chloro,

[0067] in which R⁸ is —CH₃, fluoro, in which R⁴ is fluoro, in which R⁶ is chloro or —CF₃ chloro, bromo, —CF₃, —CH₃ or chloro —N═C, —CH₃, —OCF₃ or —CH₂OH

[0068] R² has the meaning of pyridyl or the group

[0069] and

[0070] R³ has the meaning of hydrogen or fluoro, as well as their isomers and salts can be used as compound I or II in the inventive pharmaceutical composition.

[0071] These compounds have the same properties as already mentioned above under compound IV and can be used for the treatment of angiogeneous diseases. Compositions comprise compounds of general formulars I, IV and V, alone or in combination.

[0072] The above mentioned compounds are also claimed matter within the inventive combinations.

[0073] A further example for ligand binding inhibitors are peptides and DNA sequences coding for such peptides, which are used for the treatment of angiogeneous diseases. Such peptides and DNA sequences are disclosed in Seq. ID No. 1 to 59 of the sequence protocoll. It has been shown that Seq. ID Nos. 34 and 34a are of main interest.

[0074] Claimed matter of the instant invention are therefor pharmaceutical compositions

[0075] a) comprising one or several agents as compound I which modulate the biological function of one or several of the VEGF/VEGF receptor systems, and comprising one or several agents as compound II which modulate the biological function of one or several of the Angiopoietin/Tie receptor systems,

[0076] b) comprising one or several agents as compound I which are targeted to the endothelium via of one or several of the VEGF/VEGF receptor systems, and comprising one or several agents as compound II which modulate the biological function of one or several of the Angiopoietin/Tie receptor systems,

[0077] c) comprising one or several agents as compound I which modulates the biological function of one or several of the VEGF/VEGF receptor systems or of one or several of the Angiopoietin/Tie receptor systems and comprising one or several agents as compound II which are targeted to the endothelium,

[0078] d) comprising one or several agents as compound I which modulate the biological function of one or several of the VEGF/VEGF receptor systems, and comprising one or several agents as compound II which are targeted to the endothelium via one or several of the Angiopoietin/Tie receptor systems,

[0079] e) comprising one or several agents as compound I which are targeted to the endothelium via one or several of the VEGF/VEGF receptor systems, and comprising one or several agents as compound II which are targeted to the endothelium via one or several of the Angiopoietin/Tie receptor systems,

[0080] f) comprising one or several agents as compound I which modulate the biological function of one or several of the VEGF/VEGF receptor systems, and comprising one or several agents as compound II which are targeted to the endothelium via one or several of the VEGF/VEGF receptor systems,

[0081] g) comprising one or several agents as compound I which modulate the biological function of one or several of the Angiopoietin/Tie receptor systems, and comprising one or several agents as compound II which are targeted to the endothelium via one or several of the Angiopoietin/Tie receptor systems and

[0082] h) comprising one or several agents which interfere with both the function of one or several of the VEGF/VEGF receptor systems and the function of one or several of the Angiopoietin/Tie receptor systems.

[0083] For a sequential therapeutical application the inventive pharmaceutical compositions can be applied simultaneously or separately.

[0084] The inventive compositions comprise as compound I or as compound II at least one of

[0085] a) compounds which inhibit receptor tyrosine kinase activity,

[0086] b) compounds which inhibit ligand binding to receptors,

[0087] c) compounds which inhibit activation of intracellular signal pathways of the receptors,

[0088] d) compounds which inhibit or activate expression of a ligand or of a receptor of the VEGF or Tie receptor system,

[0089] e) delivery systems, such as antibodies, ligands, high-affinity binding oligonucleotides or oligopeptides, or liposomes, which target cytotoxic agents or coagulation-inducing agents to the endothelium via recognition of VEGF/VEGF receptor or Angiopoietin/Tie receptor systems,

[0090] f) delivery systems, such as antibodies, ligands, high-affinity binding oligonucleotides or oligopeptides, or liposomes, which are targeted to the endothelium and induce necrosis or apoptosis.

[0091] These compositions are also claimed matter of the present invention.

[0092] Also claimed matter of the present invention are pharmaceutical compositions which comprise as compound I and/or II at least one of Seq. ID Nos. 1-59. Of most value are pharmaceutical compositions, which comprise as compound I and/or II Seq. ID Nos. 34a und pharmaceutical compositions according to claims which comprise as compound I and/or II at least one of sTie2, mAB 4301-42-35, scFv-tTF and/or L19 scFv-tTF conjugate.

[0093] Further preferred matter of the present invention are pharmaceutical compositions, which comprise as compound I and/or II at least one small molecule of general formula I, general formula IV and/or general formula V.

[0094] The most preferred compound which can be used as compound I or II in the inventive composition is (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate.

[0095] Therefore, claimed matter of the present invention are also pharmaceutical compositions, which comprise as compound I (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate, sTie2, mAB 4301-42-35, scFv-tTF and/or L19 scFv-tTF conjugate, and as compound II (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinatesTie2, mAB 4301-42-35, scFv-tTF and/or L19 scFv-tTF conjugate, with the provisio that compound I is not identically to compound II, and most preferred pharmaceutical compositions, which comprise as compound I (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate and as compound II sTie2, mAB 4301-42-35, scFv-tTF and/or L19 scFv-tTF conjugate; pharmaceutical compositions, which comprise as compound I mAB 4301-42-35 and as compound II sTie2, and/or scFv-tTF conjugate; pharmaceutical compositions, which comprise as compound I scFv-tTF conjugate and as compound II sTie2 and/or mAB 4301-42-35; pharmaceutical compositions, which comprise as compound I L19 scFv-tTF conjugate and as compound II sTie2.

[0096] The small molecule compounds, proteins and DNA's expressing proteins, as mentioned above can be used as medicament alone, or in form of formulations for the treatment of tumors, cancers, psoriasis, arthritis, such as rheumatoide arthritis, hemangioma, angiofribroma, eye diseases, such as diabetic retinopathy, neovascular glaukoma, kidney diseases, such as glomerulonephritis, diabetic nephropathy, maligneous nephrosclerose, thrombic microangiopatic syndrome, transplantation rejections and glomerulopathy, fibrotic diseases, such as cirrhotic liver, mesangial cell proliferative diseases, artheriosclerosis and damage of nerve tissues.

[0097] The treatment of the damaged nerve tissues with the inventive combination hinders the rapid formation of scars at the damaged position. Thus, there is no scar formation before the axons communicate with each other. Therefore a reconstruction of the nerve bindings is much more easier.

[0098] Further, the inventive combinations can be used for suppression of the ascites formation in patients. It is also possible to suppress VEGF oedemas.

[0099] For the use of the inventive combinations as medicament the compounds will be formulated as pharmaceutical composition. Said formulation comprises beside the active compound or compounds acceptable pharmaceutically, organically or inorganically inert carriers, such as water, gelatine, gum arabic, lactose, starch, magnesium stearate, talcum, plant oils, polyalkylene glycols, etc. Said pharmaceutical preparations can be applied in solid form, such as tablets, pills, suppositories, capsules, or can be applied in fluid form, such as solutions, suspensions or emulsions.

[0100] If necessary, the compositions additionally contain additives, such as preservatives, stabilizer, detergents or emulgators, salts for alteration of the osmotic pressure and/or buffer.

[0101] These uses are also claimed matter of the instant invention, as well as the formulations of the active compounds

[0102] For parenteral application especially injectable solutions or suspensions are suitable, especially hydrous solutions of the active compound in polyhydroxyethoxylated castor-oil are suitable.

[0103] As carrier also additives can be used, such as salts of the gallic acid or animal or plant phospholipids, as well as mixtures thereof, and liposomes or ingredients thereof.

[0104] For oral application especially suitable are tablets, pills or capsules with talcum and/or hydrocarbon carriers or binders, such as lactose, maize or potato starch. The oral application can also be in form of a liquid, such as juice, which optionally contains a sweetener.

[0105] The dosis of the active compound differs depending on the application of the compound, age and weight of the patient, as well as the form and the progress of the disease.

[0106] The daily dosage of the active compound is 0.5-1000 mg, especially 50-200 mg. The dosis can be applied as single dose or as two or more daily dosis.

[0107] These formulations and application forms are also part of the instant invention.

[0108] Combined functional interference with VEGF/VEGF receptor systems and with Angiopoietin/Tie receptor systems can be performed simultaneously, or in sequential order such that the biological response to interference with one ligand/receptor system overlaps with the biological response to interference with a second ligand/receptor system. Alternatively, combined functional interference with VEGF/VEGF receptor systems or with Angiopoietin/Tie receptor systems and targeting of cytotoxic agents via VEGF/VEGF receptor systems or via Angiopoietin/Tie receptor systems can be performed simultaneously, or in sequential order such that the biological response to functional interference with a ligand/receptor system overlaps in time with targeting of cytotoxic agents.

[0109] The invention is also directed to a substance which functional interferes with both VEGF/VEGF receptor systems and Angiopoietin/Tie receptor systems, or which are targeted via both VEGF/VEGF receptor systems and Angiopoietin/Tie receptor systems.

[0110] VEGF/VEGF receptor systems include the ligands VEGF-A, VEGF-B, VEGF-C, VEGF-D, PIGF, and the receptor tyrosine kinases VEGF-R1 (Flt1), VEGF-R2 (KDR/Flk1), VEGF-R3 (Flt4), and their co-receptors (i.e. neuropilin-1). Angiopoietin/Tie receptor systems include Ang1, Ang2, Ang3/Ang4, and angiopoietin related polypeptides which bind to Tie1 or to Tie2, and the receptor tyrosine kinases Tie1 and Tie2.

[0111] Phamaceutical compositions of the present invention can be used for medicinal purposes. Such diseases are, for example, cancer, cancer metastasis, angiogenesis including retinopathy and psoriasis. Pharmaceutical compositions of the present invention can be applied orally, parenterally, or via gene therapeutic methods.

[0112] Therefor the present invention also concerns the use of pharmaceutical compositions for the production of a medicament for the treatment of tumors, cancers, psoriasis, arthritis, such as rheumatoide arthritis, hemangioma, angiofribroma, eye diseases, such as diabetic retinopathy, neovascular glaukoma, kidney diseases, such as glomerulonephritis, diabetic nephropathie, maligneous nephrosclerosis, thrombic microangiopatic syndrome, transplantation rejections and glomerulopathy, fibrotic diseases, such as cirrhotic liver, mesangial cell proliferative diseases, artheriosclerosis, damage of nerve tissues, suppression of the ascites formation in patients and suppression of VEGF oedemas.

[0113] The following examples demonstrate the feasability of the disclosed invention, without restricting the inventon to the disclosed examples.

EXAMPLE 1

[0114] Superior effect on inhibition of tumor growth via combination of inhibition of the VEGF A/VEGF receptor system together with functional interference with the Angiopoietin/Tie2 receptor system over separate modes of intervention was demonstrated in an A375v human melanoma xenograft model.

[0115] Human melanoma cell line A375v was stably transfected to overexpress the extracellular ligand-neutralizing domain of human Tie2 receptor tyrosine kinase (sTie2; compound II) (Siemeister et al., Cancer Res. 59, 3185-3191, 1999). For control, A375v cells were stably transfected with the empty expression vector (A375v/pCEP). Swiss nu/nu mice were s.c. injected with 1×10⁶ transfected A375v/sTie2 or A375v/pCEP tumor cells, respectively. Animals receiving compound I were treated for up to 38 days with daily oral doses of 50 mg/kg of the VEGF receptor tyrosine kinase inhibitor (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate (Wood et al., Cancer Res. 60, 2178-2189, 2000). Various modes of treatment are described in Table 1. Tumor growth was determined by caliper measurement of the largest diameter and its perpendicular. TABLE 1 mode of treatment (4-Chlorophenyl)[4-(4-pyridylmethyl)- phthalazin-1-yl]ammonium hydrogen sTie2 treatment group succinate (compound I) (compound II) Group 1: − − A375v/pCEP Group 2: + − A375v/pCEP Group 3: − + A375v/sTie2 Group 4: + + A375v/sTie2

[0116] Tumors derived from A375v/pCEP control cells reached a size of approx. 250 mm² (mean area) within 24 days (FIG. 1) without treatment (group 1). Separate treatment with the VEGF receptor inhibitor (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate (compound I, treatment group 2) or separate interference with Angiopoietin/Tie2 receptor system by means of expression of sTie2 (compound II, treatment group 3) delayed growth of tumors to a size of approx. 250 mm² to 31 days, respectively. Combination of interference with the Angiopoietin/Tie2 system by means of expression of sTie2 and of interference with the VEGF/VEGF receptor system by means of the kinase inhibitor (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate (compound I+compound II, treatment group 4) delayed growth of the tumors to a size of approx. 250 mm² to 38 days.

[0117] This result clearly demonstrates the superior effect of a combination of interference with the VEGF-A/VEGF receptor system and the Angiopoietin/Tie2 receptor system over separate modes of intervention.

EXAMPLE 2

[0118] Combination of functional interference with the Angiopoietin/Tie2 receptor system and neutralization of VEGF-A is superior to separate modes of intervention in inhibition of tumor growth.

[0119] Tumors derived from A375v/sTie2 cells and from A375v/pCEP cells were induced in nude mice as described in example 1. Animals receiving compound I were treated twice weekly over a period of time of 4 weeks with intraperitoneal doses of 200 μg of the VEGF-A-neutralizing monoclonal antibody (mAb) 4301-42-35 (Schlaeppi et al., J. Cancer Res. Clin. Oncol. 125, 336-342, 1999). Various modes of treatment are descibed in Table 2. Animals were sacrificed for ethical reasons when tumors of group 1 exceeded a volume of approx. 1000 mm³. Tumor growth was determined by caliper measurement of the largest diameter and its perpendicular. TABLE 2 mode of treatment mAb 4301-42-35 sTie2 treatment group (compound I) (compound II) Group 1: − − A375v/pCEP Group 2: + − A375v/pCEP Group 3: − + A375v/sTie2 Group 4: + + A375v/sTie2

[0120] Tumors derived from A375v/pCEP control cells reached a size of approx. 1000 mm³ within 28 days (FIG. 2) without treatment (group 1). Tumors treated with the VEGF-A-neutralizing mAb 4301-42-35 (compound I, treatment group 2) grew to a volume of approx. 450 mm³ within 28 days. Interference with Angiopoietin/Tie2 receptor system by means of expression of sTie2 (compound II, treatment group 3) reduced growth of tumors within 28 day to a volume of approx. 600 mm², respectively. Combination of interference with the Angiopoietin/Tie2 system by means of expression of sTie2 and neutralizing of VEGF-A by means of the mAb 4301-42-35 (compound I+compound II, treatment group 4) resulted in a inhibition of tumor growth to a volume of approx. 250 mm³ within 28 days.

[0121] The superior effect of a combination of neutralization of VEGF-A and functional interference with the Angiopoietin/Tie2 receptor system over separate modes of intervention is clearly shown.

EXAMPLE 3

[0122] Combination of functional interference with the Angiopoietin/Tie2 receptor system and targeting of a coagulation-inducing protein via the VEGF/VEGF receptor system is superior to separate modes of intervention in inhibition of tumor growth.

[0123] Tumors derived from A375v/sTie2 cells and from A375v/pCEP cells were induced in nude mice as described in example 1. A single chain antibody (scFv) specifically recognizing the human VEGF-A/VEGF receptor I complex (WO 99/19361) was expressed in E. coli and conjugated to coagulation-inducing recombinant human truncated tissue factor (tTF) by methods descibed by Ran et al. (Cancer Res. 58, 4646-4653, 1998). When tumors reached a size of approx. 200 mm³ animals receiving compound I were treated on day 0 and on day 4 with intravenous doses of 20 μg of the scFv-tTF conjugate. Various modes of treatment are described in Table 3. Animals were sacrificed for ethical reasons when tumors of group 1 exceeded a volume of approx. 1000 mm³. Tumor growth was determined by caliper measurement of the largest diameter and its perpendicular. TABLE 3 mode of treatment scFv-tTF conjugate sTie2 treatment group (compound I) (compound II) Group 1: − − A375v/pCEP Group 2: + − A375v/pCEP Group 3: − + A375v/sTie2 Group 4: + + A375v/sTie2

[0124] Tumors derived from A375v/pCEP control cells reached a size of approx. 1000 mm³ within 28 days (FIG. 3) without treatment (group 1). Tumors treated with the coagulation-inducting tTF targeted to the VEGF-A/VEGF receptor I complex via the scFv-tTF conjugate (compound I, treatment group 2) grew to a volume of approx. 500 mm³ within 28 days. Interference with Angiopoietin/Tie2 receptor system by means of expression of sTie2 (compound II, treatment group 3) reduced growth of tumors within 28 day to a volume of approx. 600 mm², respectively. Combination of interference with the Angiopoietin/Tie2 system by means of expression of sTie2 and of targeting the VEGF receptor complex (compound I+compound II, treatment group 4) resulted in a inhibition of tumor growth to a volume of approx. 300 mm³ within 28 days.

[0125] The superior effect of a combination of targeting of the coagulation-inducting tTF to the VEGF-A/VEGF receptor I complex and functional interference with the Angiopoietin/Tie2 receptor system over separate modes of intervention is clearly shown. Similar effects can be expected upon targeting of cytotoxic agents to VEGF/VEGF receptor systems.

EXAMPLE 4

[0126] Combination of functional interference with the VEGF/VEGF receptor system and targeting of a coagulation-inducing protein via the VEGF/VEGF receptor system is superior to separate modes of intervention in inhibition of tumor growth.

[0127] Tumors derived from A375v/pCEP cells were induced in nude mice as described in example 1. Animals receiving compound I were treated for up to 28 days with daily oral doses of 50 mg/kg of the VEGF receptor tyrosine kinase inhibitor (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate (Wood et al., Cancer Res. 60, 2178-2189, 2000). Compound II consists of a single chain antibody (scFv) specifically recognizing the human VEGF-A/VEGF receptor I complex (WO 99/19361) which was expressed in E. coli and conjugated to coagulation-inducing recombinant human truncated tissue factor (tTF) by methods descibed by Ran et al. (Cancer Res. 58, 4646-4653, 1998). When tumors reached a size of approx. 200 mm³ animals receiving compound II were treated on day 0 and on day 4 with intravenous doses of 20 μg of the scFv-tTF conjugate. Various modes of treatment are described in Table 4. Animals were sacrificed for ethical reasons when tumors of group 1 exceeded a volume of approx. 1000 mm³. Tumor growth was determined by caliper measurement of the largest diameter and its perpendicular. TABLE 4 mode of treatment (4-Chlorophenyl)[4-(4-pyridylmethyl)- phthal-azin-1-yl]ammonium hydrogen scFv-tTF succinate conjugate treatment group (compound I) (compound II) Group 1: − − A375v/pCEP Group 2: + − A375v/pCEP Group 3: − + A375v/pCEP Group 4: + + A375v/pCEP

[0128] Tumors derived from A375v/pCEP control cells reached a size of approx. 1000 mm³ within 28 days (FIG. 4) without treatment (group 1). Separate treatment with the VEGF receptor inhibitor (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate (compound I, treatment group 2) resulted in a reduction of the tumor volumes to approx. 550 mm³. Tumors treated with the coagulation-inducting tTF targeted to the VEGF-A/VEGF receptor I complex via the scFv-tTF conjugate (compound II, treatment group 3) grew to a volume of approx. 500 mm³ within 28 days. Combination of inhibition of VEGF receptor tyrosine kinase by means of (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate and of targeting the VEGF receptor complex (compound I+compound II, treatment group 4) resulted in a inhibition of tumor growth to a volume of approx. 400 mm³ within 28 days.

[0129] The superior effect of a combination of targeting of the coagulation-inducting tTF to the VEGF-A/VEGF receptor I complex and functional interference with the VEGF/VEGF receptor system over separate modes of intervention is clearly shown. Similar effects can be expected upon targeting of cytotoxic agents to Angiopoietin/Tie receptor systems.

EXAMPLE 5

[0130] Combination of functional interference with the Angiopoietin/Tie2 receptor system and endothelium-specific targeting of a coagulation-inducing protein is superior to separate modes of intervention in inhibition of tumor growth.

[0131] Tumors derived from A375v/sTie2 cells and from A375v/pCEP cells were induced in nude mice as described in example 1. A fusion protein (L19 scFv-tTF) consisting of L19 single chain antibody specifically recognizing the oncofoetal ED-B domain of fibronectin and the extracellular domain of tissue factor was expressed in E. coli as described by Nilsson et al. (Nat. Med., in press). Further, L19 scFv-tTF data have been represented by D. Neri and F. Nilsson (Meeting “Advances in the application of monoclonal antibodies in clinical oncology”, Samos, Greece, 31. May-2. June 2000). When tumors reached a size of approx. 200 mm³ animals receiving compound I were treated with a single intravenous dose of 20 μg of L19 scFv-tTF in 200 μl saline. Various modes of treatment are described in Table 5. Animals were sacrificed for ethical reasons when tumors of group 1 exceeded a volume of approx. 1000 mm³. Tumor growth was determined by caliper measurement of the largest diameter and its perpendicular. TABLE 5 mode of treatment L19 scFv-tTF sTie2 treatment group (compound I) (compound II) Group 1: − − A375v/pCEP Group 2: + − A375v/pCEP Group 3: − + A375v/sTie2 Group 4: + + A375v/sTie2

[0132] Tumors derived from A375v/pCEP control cells reached a size of approx. 1000 mm³ within 28 days (FIG. 5) without treatment (group 1). Tumors treated with the coagulation-inducting L19 scFv-tTF (compound I, treatment group 2) grew to a volume of approx. 450 mm³ within 28 days. Interference with Angiopoietin/Tie2 receptor system by means of expression of sTie2 (compound II, treatment group 3) reduced growth of tumors within 28 day to a volume of approx. 600 mm², respectively. Combination of interference with the Angiopoietin/Tie2 system by means of expression of sTie2 and of targeting the endothelium with L19 scFv-tTF (compound I+compound II, treatment group 4) resulted in a inhibition of tumor growth to a volume of approx. 250 mm³ within 28 days.

[0133] The superior effect of a combination of targeting of L19 scFv-tTF to the endothelium and functional interference with the Angiopoietin/Tie2 receptor system over separate modes of intervention is clearly shown.

EXAMPLE 6

[0134] Combination of functional interference with the VEGF/VEGF receptor system and endothelium-specific targeting of a coagulation-inducing protein is superior to separate modes of intervention in inhibition of tumor growth.

[0135] Tumors derived from A375v/pCEP cells were induced in nude mice as described in example 1. Animals receiving compound I were treated for up to 28 days with daily oral doses of 50 mg/kg of the VEGF receptor tyrosine kinase inhibitor (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate (Wood et al., Cancer Res. 60, 2178-2189, 2000). Compound II consists of L19 scFv-tTF fusion protein as described in example 5. When tumors reached a size of approx. 200 mm³ animals receiving compound II were treated with a single intravenous dose of 20 μg of L19 scFv-tTF in 200 μl saline. Various modes of treatment are described in Table 6. Animals were sacrificed for ethical reasons when tumors of group 1 exceeded a volume of approx. 1000 mm³. Tumor growth was determined by caliper measurement of the largest diameter and its perpendicular. TABLE 6 mode of treatment (4-Chlorophenyl)[4-(4-pyridylmethyl)- phthal-azin-1-yl]ammonium hydrogen succinate L19 scFv-tTF treatment group (compound I) (compound II) Group 1: − − A375v/pCEP Group 2: + − A375v/pCEP Group 3: − + A375v/pCEP Group 4: + + A375v/pCEP

[0136] Tumors derived from A375v/pCEP control cells reached a size of approx. 1000 mm³ within 28 days (FIG. 6) without treatment (group 1). Separate treatment with the VEGF receptor inhibitor (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate (compound I, treatment group 2) resulted in a reduction of the tumor volumes to approx. 550 mm³. Tumors treated with the coagulation-inducting L19 scFv-tTF targeted to the endothelium (compound II, treatment group 3) grew to a volume of approx. 450 mm³ within 28 days. Combination of inhibition of VEGF receptor tyrosine kinase by means of (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate and of targeting the VEGF receptor complex (compound I+compound II, treatment group 4) resulted in a inhibition of tumor growth to a volume of approx. 200 mm³ within 28 days.

[0137] The superior effect of a combination of targeting of L19 scFv-tTF to the endothelium and functional interference with the VEGF/VEGF receptor system over separate modes of intervention is clearly shown.

DESCRIPTION OF THE FIGURES

[0138]FIG. 1 shows the superior effect of combination of interference with VEGF/VEGF receptor system by means of an specific tyrosine kinase inhibitor and with the Angiopoietin/Tie2 receptor system by means of a soluble receptor domain on inhibition of tumor growth (treatment modes of groups 1-4 are given in Table 1). The abbreviations have the following meaning: mock, con. = treatment group 1 mock + VEGF-A = treatment group 2 sTIE2-cl13 = treatment group 3 sTIE2-cl13 + VEGF-A = treatment group 4

[0139]FIG. 2 shows the superior effect on tumor growth inhibition of combination of VEGF-neutralization and functional interference with Angiopoietin/Tie2 receptor system over separate modes of intervention (treatment modes of groups 1-4 are given in Table 2).

[0140]FIG. 3 shows the superior effect on tumor growth inhibition of combination of targeting of the coagulation-inducing tTF to the VEGF/VEGF receptor I complex via a scFv-tTF conjugate and functional interference with Angiopoietin/Tie2 receptor system over separate modes of intervention (treatment modes of groups 1-4 are given in Table 3).

[0141]FIG. 4 shows the superior effect on tumor growth inhibition of combination of targeting of the coagulation-inducing tTF to the VEGF/VEGF receptor I complex via a scFv-tTF conjugate and functional interference with VEGF/VEGF receptor system by means of the VEGF receptor tyrosine kinase inhibitor (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate over separate modes of intervention (treatment modes of groups 1-4 are given in Table 4).

[0142]FIG. 5 shows the superior effect on tumor growth inhibition of combination of targeting of the coagulation-inducing L19 scFv-tTF fusion protein to the endothelium and functional interference with Angiopoietin/Tie2 receptor system over separate modes of intervention (treatment modes of groups 1-4 are given in Table 5).

[0143]FIG. 6 shows the superior effect on tumor growth inhibition of combination of targeting of the coagulation-inducing L19 scFv-tTF fusion protein to the endothelium and functional interference with VEGF/VEGF receptor system by means of the VEGF receptor tyrosine kinase inhibitor (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate over separate modes of intervention (treatment modes of groups 1-4 are given in Table 6).

1 60 1 1835 DNA Homo sapiens 1 ttttacagtt ttccttttct tcagagttta ttttgaattt tcatttttgg ataaccaagc 60 agctctttaa gaagaatgca cagaagagtc attctggcac ttttggatag tacataagat 120 tttctttttt ttttttaaat tttttttaat agtcacattc agctcgcttg ctcaaaccag 180 actcccacat tgggtgagca agatgagccc ataggattcc agagttaata cgtaaccgta 240 tatacaaaca gccaaaaaac cataatggtg ccacagggat ggagcaggga agggcatctc 300 taacgtgtcc tctagtctat cttcgctaaa cagaacccac gttacacatg ataactagag 360 agcacactgt gttgaaacga ggatgctgac cccaaatggc acttggcagc atgcagttta 420 aagcaaaaga gacatccttt aataactgta taaaatccag gcagttccat taaaggggtt 480 aagaaaacca acaacaacaa aaagcgaggg actgtctgtt gtcactgtca aaaaggcact 540 tggagttaat gggaccagga ttggaggact cttagctgat acagatttca gtacgatttc 600 attaaaaggc ttggatgtta agagaggaca ctcagcggtt cctgaaggga gacgctgaga 660 tggaccgctg agaagcggaa cagatgaaca caaaggaatc aaatctttac aaccaaattg 720 catttaagcg acaacaaaaa aaggcaaacc ccaaaacgca acctaaccaa agcaaaatct 780 aagcaaaatc agacaacgaa gcagcgatgc atagctttcc tttgagagaa cgcatacctt 840 gagacgctac gtgccaacct aagttctcaa cgacagcttc acagtaggat tattgtgata 900 aaaatgactc aagcgatgca aaaagtttca tctgttccca gaatccgagg gagaactgag 960 gtgatcgtta gagcatagcg acatcacgtg cggtttctta atgtccctgg tggcggatac 1020 gccgagtcct cggaaggaca tctggacacc actttcagcc acctccttgc aggggcgaca 1080 tccgccaaag tcatccttta ttccgagtaa taactttaat tcctttctaa catttacacg 1140 gcaaacagga atgcagtaaa cgtccacgtc cgtcccacgg ctgggctgcc gttccgtttc 1200 ctccacgaac gggtacgcgc ttccatgaga aaggatattt ggcaatttta tattccacag 1260 tcaggtgggt ctgcgatagc tcatttaatg ttaaacgcca tcaggggcct ctcctcccgt 1320 ttctgccagg ggcttttctt gtcttctcct tggcgagctc gtgggcagat cttctctggt 1380 gggggctggc tgctggctcc gagggggcat ccgcagtccg tctggtcgtc tcctcctgca 1440 ggctgggcag ctggccacca cttctccgac tcgacccctc caacaagcat cgcagggcac 1500 tgtcctcggg ggtacagacc gtggtcccac attcgctacc actctgttcc acgtcatcca 1560 ggtacacgag ctgcgtgtag gccgtgctgt ctggggctcg aggctctttc tgctggtgct 1620 cttggacggg cgggtagttc tgctgcagag acaaagcatc tccccttccc ttccgggctg 1680 attttggttc attcatatct acgccagagt ccaaactggc atcattactt ccgttccttc 1740 cagctctttg gagaatcaat gtatgaatgt ctaacctgac cgttggacct gccatccaag 1800 gagacgaacc acgcccgggg gtgcggaagc ggcct 1835 2 581 DNA Homo sapiens 2 gttctagatt gttttattca gtaattagct cttaagaccc ctggggcctg tgctacccag 60 acactaacaa cagtctctat ccagttgctg gttctgggtg acgtgatctc cccatcatga 120 tcaacttact tcctgtggcc cattagggaa gtggtgacct cgggagctat ttgcctgttg 180 agtgcacaca cctggaaaca tactgctctc attttttcat ccacatcagt gagaaatgag 240 tggcccgtta gcaagatata actatgcaat catgcaacaa agctgcctaa taacatttca 300 tttattacag gactaaaagt tcattattgt ttgtaaagga tgaattcata acctctgcag 360 agttatagtt catacacagt tgatttccat ttataaaggc agaaagtcct tgttttctct 420 aaatgtcaag ctttgactga aaactcccgt ttttccagtc actggagtgt gtgcgtatga 480 aagaaaatct ttagcaatta gatgggagag aagggaaata gtacttgaaa tgtaggccct 540 cacctcccca tgacatcctc catgagcctc ctgatgtagt g 581 3 516 DNA Homo sapiens 3 tagagatgtt ggttgatgac ccccgggatc tggagcagat gaatgaagag tctctggaag 60 tcagcccaga catgtgcatc tacatcacag aggacatgct catgtcgcgg aacctgaatg 120 gacactctgg gttgattgtg aaagaaattg ggtcttccac ctcgagctct tcagaaacag 180 ttgttaagct tcgtggccag agtactgatt ctcttccaca gactatatgt cggaaaccaa 240 agacctccac tgatcgacac agcttgagcc tcgatgacat cagactttac cagaaagact 300 tcctgcgcat tgcaggtctg tgtcaggaca ctgctcagag ttacaccttt ggatgtggcc 360 atgaactgga tgaggaaggc ctctattgca acagttgctt ggcccagcag tgcatcaaca 420 tccaagatgc ttttccagtc aaaagaacca gcaaatactt ttctctggat ctcactcatg 480 atgaagttcc agagtttgtt gtgtaaagtc cgtctg 516 4 1099 DNA Homo sapiens 4 cccacaacac aggggccctg aaacacgcca gcctctcctc tgtggtcagc ttggcccagt 60 cctgctcact ggatcacagc ccattgtagg tggggcatgg tggggatcag ggcccctggc 120 ccacggggag gtagaagaag acctggtccg tgtaagggtc tgagaaggtg ccctgggtcg 180 ggggtgcgtc ttggccttgc cgtgccctca tcccccggct gaggcagcga cacagcaggt 240 gcaccaactc cagcaggtta agcaccaggg agatgagtcc aaccaccaac atgaagatga 300 tgaagatggt cttctccgtg gggcgagaga caaagcagtc cacgaggtag gggcagggtg 360 ctcgctggca cacaaacacg ggctccatgg tccagccgta caggcgccac tggccataga 420 ggaagcctgc ctctagcaca ctcttgcaga gcacactggc gacataggtg cccatcagtg 480 ctccgcggat gcgcaggcga ccatcttctg ccaccgagat cttggccatc tgacgctcta 540 cggccgccag cgcccgctcc acctgtgggt ccttggccgg cagtgcccgc agctccccct 600 ccttctgccg cagccgctct tctcgccgag acaggtaaat gacatggccc aggtagacca 660 gggtgggtgt gctgacgaag aggaactgca gcacccagta gcggatgtgg gagatgggga 720 aggcctggtc atagcagacg ttggtgcagc ctggctgggc cgtgttacac tcgaaatctg 780 actgctcgtc accccacact gactcgccgg ccaggcccag gatgaggatg cggaagatga 840 agagcaccgt cagccagatc ttacccacca cggtcgagtg ctcctggacc tggtccagca 900 acttctccac gaagccccag tcacccatgg ctcccgggcc tccgtcggca aggagacaga 960 gcacgtcagt gtgtcagcat ggcatccttc tcgttcgccc agcaacaagc ctgcagggag 1020 gtctgccacg cccgttctac cgcctgcctg ccgggcggcc caggtggagg tggggacgat 1080 ggccggagtg acgcccgcg 1099 5 1015 DNA Homo sapiens 5 gaggataggg agcctggggt caggagtgtg ggagacacag cgagactctg tctccaaaaa 60 aaaaagtgct ttttgaaaat gttgaggttg aaatgatggg aaccaacatt ctttggattt 120 agtggggagc ataatagcaa acaccccctt ggttcgcaca tgtacaggaa tgggacccag 180 ttggggcaca gccatggact tccccgccct ggaatgtgtg gtgcaaagtg gggccagggc 240 ccagacccaa gaggagaggg tggtccgcag acaccccggg atgtcagcat cccccgacct 300 gccttctggc ggcacctccc gggtgctgtg ttgagtcagc aggcatgggg tgagagcctg 360 gtatatgctg ggaacagggt gcaggggcca agcgttcctc cttcagcctt gacttgggcc 420 atgcaccccc tctcccccaa acacaaacaa gcacttctcc agtatggtgc caggacaggt 480 gtcccttcag tcctctggtt atgacctcaa gtcctacttg ggccctgcag cccagcctgt 540 gttgtaacct ctgcgtcctc aagaccacac ctggaagatt cttcttccct ttgaaggaga 600 atcatcattg ttgctttatc acttctaaga cattttgtac ggcacggaca agttaaacag 660 aatgtgcttc cctccctggg gtctcacacg ctcccacgag aatgccacag gggccgtgca 720 ctgggcaggc ttctctgtag aaccccaggg gcttcggccc agaccacagc gtcttgccct 780 gagcctagag cagggagtcc cgaacttctg cattcacaga ccacctccac aattgttata 840 accaaaggcc tcctgttctg ttatttcact taaatcaaca tgctattttg ttttcactca 900 cttctgactt tagcctcgtg ctgagccgtg tatccatgca gtcatgttca cgtgctagtt 960 acgtttttct tcttacacat gaaaataaat gcataagtgt tagaagaaaa aaaaa 1015 6 2313 DNA Homo sapiens 6 ccagagcagg cctggtggtg agcagggacg gtgcaccgga cggcgggatc gagcaaatgg 60 gtctggccat ggagcacgga gggtcctacg ctcgggcggg gggcagctct cggggctgct 120 ggtattacct gcgctacttc ttcctcttcg tctccctcat ccaattcctc atcatcctgg 180 ggctcgtgct cttcatggtc tatggcaacg tgcacgtgag cacagagtcc aacctgcagg 240 ccaccgagcg ccgagccgag ggcctataca gtcagctcct agggctcacg gcctcccagt 300 ccaacttgac caaggagctc aacttcacca cccgcgccaa ggatgccatc atgcagatgt 360 ggctgaatgc tcgccgcgac ctggaccgca tcaatgccag cttccgccag tgccagggtg 420 accgggtcat ctacacgaac aatcagaggt acatggctgc catcatcttg agtgagaagc 480 aatgcagaga tcaattcaag gacatgaaca agagctgcga tgccttgctc ttcatgctga 540 atcagaaggt gaagacgctg gaggtggaga tagccaagga gaagaccatt tgcactaagg 600 ataaggaaag cgtgctgctg aacaaacgcg tggcggagga acagctggtt gaatgcgtga 660 aaacccggga gctgcagcac caagagcgcc actggccaag gagcaactgc aaaaggtgca 720 agccctctgc ctgcccctgg acaaggacaa gtttgagatg gaccttcgta acctgtggag 780 ggactccatt atcccacgca gcctggacaa cctgggttac aacctctacc atcccctggg 840 ctcggaattg gcctccatcc gcagagcctg cgaccacatg cccagcctca tgagctccaa 900 ggtggaggag ctggcccgga gcctccgggc ggatatcgaa cgcgtggccc gcgagaactc 960 agacctccaa cgccagaagc tggaagccca gcagggcctg cgggccagtc aggaggcgaa 1020 acagaaggtg gagaaggagg ctcaggcccg ggaggccaag ctccaagctg aatgctcccg 1080 gcagacccag ctagcgctgg aggagaaggc ggtgctgcgg aaggaacgag acaacctggc 1140 caaggagctg gaagagaaga agagggaggc ggagcagctc aggatggagc tggccatcag 1200 aaactcagcc ctggacacct gcatcaagac caagtcgcag ccgatgatgc cagtgtcaag 1260 gcccatgggc cctgtcccca acccccagcc catcgaccca gctagcctgg aggagttcaa 1320 gaggaagatc ctggagtccc agaggccccc tgcaggcatc cctgtagccc catccagtgg 1380 ctgaggaggc tccaggcctg aggaccaagg gatggcccga ctcggcggtt tgcggaggat 1440 gcagggatat gctcacagcg cccgacacaa ccccctcccg ccgcccccaa ccacccaggg 1500 ccaccatcag acaactccct gcatgcaaac ccctagtacc ctctcacacc cgcacccgcg 1560 cctcacgatc cctcacccag agcacacggc cgcggagatg acgtcacgca agcaacggcg 1620 ctgacgtcac atatcaccgt ggtgatggcg tcacgtggcc atgtagacgt cacgaagaga 1680 tatagcgatg gcgtcgtgca gatgcagcac gtcgcacaca gacatgggga acttggcatg 1740 acgtcacacc gagatgcagc aacgacgtca cgggccatgt cgacgtcaca catattaatg 1800 tcacacagac gcggcgatgg catcacacag acggtgatga tgtcacacac agacacagtg 1860 acaacacaca ccatgacaac gacacctata gatatggcac caacatcaca tgcacgcatg 1920 ccctttcaca cacactttct acccaattct cacctagtgt cacgttcccc cgaccctggc 1980 acacgggcca aggtacccac aggatcccat cccctcccgc acagccctgg gccccagcac 2040 ctcccctcct ccagcttcct ggcctcccag ccacttcctc acccccagtg cctggacccg 2100 gaggtgagaa caggaagcca ttcacctccg ctccttgagc gtgagtgttt ccaggacccc 2160 ctcggggccc tgagccgggg gtgagggtca cctgttgtcg ggaggggagc cactccttct 2220 cccccaactc ccagccctgc ctgtggcccg ttgaaatgtt ggtggcactt aataaatatt 2280 agtaaatcct taaaaaaaaa aaaaaaaaaa aaa 2313 7 389 DNA Homo sapiens 7 gccaaaaaga tggcttcaaa agtaagaatg aaacatttga tccattcagc tttaggctat 60 gccactggat tcatgtctag aaaagatagg ataatttctg taaagaaatg aagaccttgc 120 tattctaaaa tcagatcctt acagatccag atttcaggaa acaaatacat aggggactaa 180 ctttccttgt tcagattagt ttttctcctt tgcacccagc tatataatat gaggaagtat 240 tgacttttta aaagtgtttt agttttccat ttctttgata tgaaaagtaa tatttcggga 300 gaaccctgag ctattaataa tctatgtggc tagtgcgtat atattggtct gaatttgttc 360 tccttttgtg gtgtccagtg ggtaacatc 389 8 157 DNA Homo sapiens 8 tgctttaaac agctgtgtca aaaactgaca tcagagagta aattgaattt ggttttgtag 60 gaagcaggaa gcaagcccac tcaaacgtga aatttggcat gagggatcca gtaactttct 120 cctcaatctg tgaactatat gtgagtttga tattttg 157 9 561 DNA Homo sapiens 9 aatagtcaaa acataaacaa aagctaatta actggcactg ttgtcacctg agactaagtg 60 gatgttgttg gctgacatac aggctcagcc agcagagaaa gaattctgaa ttccccttgc 120 tgaactgaac tattctgtta catatggttg acaaatctgt gtgttatttc ttttctacct 180 accatattta aatttatgag tatcaaccga ggacatagtc aaaccttcga tgatgaacat 240 tcctgatttt ttgcctgatt aatctctgtt gagctctact tgtggtcatt caagatttta 300 tgatgttgaa aggaaaagtg aatatgacct ttaaaaattg tattttgggt gatgatagtc 360 tcaccactat aaaactgtca attattgcct aatgttaaag atatccatca ttgtgattaa 420 ttaaacctat aatgagtatt cttaatggag aattcttaat ggatggatta tcccctgatc 480 ttttctttaa aatttctctg cacacacagg acttctcatt ttccaataaa tgggtgtact 540 ctgccccaat ttctaggaaa a 561 10 1508 DNA Homo sapiens 10 cacaaacacg agagactcca cggtctgcct gagcaccgcc agcctcctag gctccagcac 60 tcgcaggtcc attcttctgc acgagcctct ctgtccagat ccataagcac ggtcagctca 120 gggtcgcgga gcagtacgag gacaagtacc agcagcagct cctctgaaca gagactgcta 180 ggatcatcct tctcctccgg gcctgttgct gatggcataa tccgggtgca acccaaatct 240 gagctcaagc caggtgagct taagccactg agcaaggaag atttgggcct gcacgcctac 300 aggtgtgagg actgtggcaa gtgcaaatgt aaggagtgca cctacccaag gcctctgcca 360 tcagactgga tctgcgacaa gcagtgcctt tgctcggccc agaacgtgat tgactatggg 420 acttgtgtat gctgtgtgaa aggtctcttc tatcactgtt ctaatgatga tgaggacaac 480 tgtgctgaca acccatgttc ttgcagccag tctcactgtt gtacacgatg gtcagccatg 540 ggtgtcatgt ccctcttttt gccttgttta tggtgttacc ttccagccaa gggttgcctt 600 aaattgtgcc aggggtgtta tgaccgggtt aacaggcctg gttgccgctg taaaaactca 660 aacacagttt gctgcaaagt tcccactgtc ccccctagga actttgaaaa accaacatag 720 catcattaat caggaatatt acagtaatga ggattttttc tttctttttt taatacacat 780 atgcaaccaa ctaaacagtt ataatcttgg cactgttaat agaaagttgg gatagtcttt 840 gctgtttgcg gtgaaatgct ttttgtccat gtgccgtttt aactgatatg cttgttagaa 900 ctcagctaat ggagctcaaa gtatgagata cagaacttgg tgacccatgt attgcataag 960 ctaaagcaac acagacactc ctaggcaaag tttttgtttg tgaatagtac ttgcaaaact 1020 tgtaaattag cagatgactt ttttccattg ttttctccag agagaatgtg ctatattttt 1080 gtatatacaa taatatttgc aactgtgaaa aacaagtggt gccatactac atggcacaga 1140 cacaaaatat tatactaata tgttgtacat tcggaagaat gtgaatcaat cagtatgttt 1200 ttagattgta ttttgcctta cagaaagcct ttattgtaag actctgattt ccctttggac 1260 ttcatgtata ttgtacagtt acagtaaaat tcaaccttta ttttctaatt ttttcaacat 1320 attgtttagt gtaaagaata tttatttgaa gttttattat tttataaaaa agaatattta 1380 ttttaagagg catcttacaa attttgcccc ttttatgagg atgtgatagt tgctgcaaat 1440 gaggggttac agatgcatat gtccaatata aaatagaaaa tatattaacg tttgaaatta 1500 aaaaaaaa 1508 11 389 DNA Homo sapiens 11 gggcaggtga tcagggcaca catttcccgt ccattgagac agtagcattc ccggcaccca 60 tcgtgccagc tctcctcatt tttatgatga tgaccatcca cggtgagaca agtgcccgac 120 aggatgggtg gcccagctga agcacaggcc gctctgcact tgcagataag acagccgtga 180 ctgtcctgct ggaaacccaa ggggcagatc ttactgcatg agagctctgg acatttctta 240 cagcgacaga tgtcacagcc gtgcttattc ttcagcaatc caagtggaca atacttgtca 300 cagattatgg gtctgcactt cttgggcctt gggcggcact cacagatctc acagttttgg 360 acctcggccg cgaccacgct gggtaccga 389 12 981 DNA Homo sapiens 12 tttttttttt ttggattgca aaaatttatt aaaattggag acactgtttt aatcttcttg 60 tgccatgaga ctccatcagg cagtctacaa agaccactgg gaggctgagg atcacttgag 120 cccagaagtt tgaggctgta gtaagcttca aaggccactg cactctagct tgggtgaggc 180 aagacccttt caagcagtaa gctgcatgct tgcttgttgt ggtcattaaa aaccctagtt 240 taggataaca acatattaat cagggcaaaa tacaaatgtg tgatgcttgt tagtagagta 300 acctcagaat caaaatggaa cggttttaca gtgatatcat tatatttcat ttggcagaat 360 cattacatca ttggttacac tgaaaatcat cacatgtacc aaaagctgac tcacctagtt 420 taggataaca ggtctgcctg tttgaagatg aaaaataata cccatttaaa atttgcccta 480 ctcaatttcc ttctcagtca cattttaact tttaaacagc taatcactcc catctacaga 540 ttaaggtgta tatgccacca aaaccttttg ccaccttaaa aatttccttc aaagtttaaa 600 ctaatgcctg catttcttca atcatgaatt ctgagtcctt tgcttcttta aaacttgctc 660 cacacagtgt agtcaagccg actctccata cccaagcaag tcatccatgg ataaaaacgt 720 taccaggagc agaaccatta agctggtcca ggcaagttgg actccaccat ttcaacttcc 780 agctttctgt ctaatgcctg tgtgccaatg gcttgagtta ggcttgctct ttaggacttc 840 agtagctatt ctcatccttc cttggggaca caactgtcca taaggtgcta tccagagcca 900 cactgcatct gcacccagca ccatacctca caggagtcga ctcccacgag ccgcctgtat 960 ataagagttc ttttgatgac g 981 13 401 DNA Homo sapiens 13 ataactacag cttcagcaga caactaaaga gactgcatta aggtgatttc tctggctata 60 aagagagccc ggccgcagag catgtgactg ctgggacctc tgggataggc aacactgccc 120 tctctccccc agagcgaccc cccgggcagg tcggggccca aggaatgacc cagcaactgc 180 tccctaccca gcacactctc tttactgcca cctgcaatta tgctgtgaag atgactgggt 240 gtggtcatca cgattcagag aaatcaagat ctatgaccat tttaggcaaa gagagaaact 300 tggagaattg ctgaggacta ctgaaccttg ttttgctttt ttaaaaaata ctaaatcctc 360 acttcagcat atttagttgt cattaaaatt aagctgatat t 401 14 1002 DNA Homo sapiens 14 gacaatataa aaagtggaaa caagcataaa ttgcagacat aaaataatct tctggtagaa 60 acagttgtgg agaacaggtt gagtagagca acaacaacaa aagcttatgc agtcaccttc 120 tttgaaaatg ttaaatacaa gtcctattct ctttgtccag ctgggtttag ctagaggtag 180 ccaattactt ctcttaaggt ccatggcatt cgccaggatt ctataaaagc caagttaact 240 gaagtaaata tctggggccc atcgcacccc cactaagtac tttgtcacca tgttgtatct 300 taaaagtcat ttttcactgt ttgactcaga atttgggact tcagagtcaa acttcattgc 360 ttactccaaa cccagtttaa ttccccactt ttttaagtag gcttagcttt gagtgatttt 420 tggctataac cgaaatgtaa atccaccttc aaacaacaaa gtttgacaag actgaaatgt 480 tactgaaaac aatggtgcca tatgctccaa agacatttcc ccaagataac tgccaaagag 540 tttttgagga ggacaatgat catttattat gtaggagcct tgatatctct gcaaaataga 600 attaatacag ctcaaatgga gtagtaacca agcttttctg cccaggaagt aacaaacatc 660 actacgaaca tgagagtaca agaggaaact ttcataatgc attttttcat tcatacattc 720 attcaataaa cattagccaa gctaatgtcc caagccactg tgccaggtat taacaatata 780 acaacaataa aagacacagt ccttcctctc aaggtgttca gtctagtagg gaagatgatt 840 attcattaaa atttttggtg catcagaatc atgaggagct tgtcaaaaat gtaaattcct 900 gcctatgttc tcagatattc tggttaggtc aggagtggga acccaaaatc aattctttta 960 acaaacacta aaggtgattc taacacaggc ggtgtgagga cc 1002 15 280 DNA Homo sapiens 15 cgaggtgggc cacccgtgtc tggtctgaga tttttaaatg aggattacat tatcctattt 60 ataatattcc tattctaatc tattgtattc ttacaattaa atgtatcaaa taattcttaa 120 aaacattatt agaaacaaac tgcctaatac cttataagac taaaaaaatc accaagatga 180 aactgtatta tgactctcaa tatttaaaca tttaaaaaaa tgttagtgtt tgttaagcac 240 caatcttaac tatttcacct gcccgggcgg ccgctcgagg 280 16 2041 DNA Homo sapiens 16 ccccccgcag aactcccccc tggaatagga tttttaaaac ccttgacaat tagaaatcct 60 atagaggtta gcatttttta ggtaaaaata tggttgcccc tacagggatc atgcaacttc 120 cttaaaacca attcagcaca tatgtataaa gaaccctttt taaaaacatt tgtacttgaa 180 atacagacac agtgatgctg aagacactaa acaaaaactg aaaagtacta taccttgata 240 aattttgtta ttgccttctt tagagacttt ataatctcta gttgattttc aaggacttga 300 atttaataat ggggtaatta cacaagacgt aaaggatttt ttaaaaacaa gtattttttt 360 ttacctctag catcaattct tttataaaga atgctaaata aattacattt tttgttcagt 420 aaaactgaag atagaccatt taaatgcttc taccaaattt aacgcagctt aattagggac 480 caggtacata ttttcttctg aacatttttg gtcaagcatg tctaaccata aaagcaaatg 540 gaattttaag aggtagattt tttttccatg atgcattttg ttaataaatg tgtcaagaaa 600 ataaaaacaa gcactgagtg tgttctcttg aagtataagg gtctaatgaa aaataaaaga 660 tagatatttg ttatagtctg acattttaac agtcatagta ttagacgttt cgtgaccagt 720 gcattttgga ctctctcagg atcaaaatac gagtctgcca actgtattaa atcctcctcc 780 accccctcca ccagttggtc cacagcttcc tggtgggtcg ttgtcatcaa atccattggg 840 ccgaaatgaa catgaagcag atgcagcttg gagggcccgg gctcgagcat tcaactcttg 900 ttcctgtaaa tatagtttat tgtcttttgt tatagcatcc ataagttctt tctgtagagg 960 tgggtctcca tttatccaga gtccactggt tgggttatta ccacttaaac cattagtact 1020 atgctgtttt ttatacaaaa gcacataagc tgtgtccttt ggaaacctgc tcgtaatttt 1080 ctggactgac tgaaatgaag taaatgtcac tctactgtca ttaaataaaa acccattctt 1140 ttgacatttc cttattttcc aaatcctgtt caaaaactgc actgggacta tctctcccta 1200 gtaaatgact ctgggaggat gctaatgcca gagcctcaga ctggtggtac atctgatatg 1260 aagagtctgt acttgtgata tttctggcat aagaatagta atgcccactt tcagaggata 1320 taccagagtg aaccacaacg gaacttaata gatagggcac caattttgtg caggaagctt 1380 catcagtccc tgaaggcttt aattttttag caaggttctc actaagatca gtgaagtcaa 1440 catctacaga ccaactttct gacaatgaag agaaagaagt aattcttcta actggcaact 1500 ccaaaaccag tggccagtga tacattgtct aaaattttcc ttctcacatg atacttctga 1560 tcatatgaaa atctcaggag agtaagaata aggtattcag gttcctccgt gatttgcata 1620 gttttctcag cattttgcag agaggcacag ttttcacaat aatattggtt atcaccagta 1680 agaatctctg gagcccaaaa aataatttag taagtcagtt actgaaggtg tggtttcacc 1740 tcccggtttc tgaggtacat ctttattaac aagaatcttg ttagattcgt tagggacaga 1800 agtgttttca gaacagtaaa actcattagg aggactgcct atggtttttt cattcacaag 1860 tgagtcacag atgaaggcag ctgttgttgg attataaact actggctctt ctgaaggacc 1920 gggtacagac gcttgcatta gaccaccatc ttgtatactg ggtgatgatg ctggatcttg 1980 gacagacatg ttttccaaag aagaggaagc acaaaacgca agcgaaagat ctgtaaaggc 2040 t 2041 17 235 DNA Homo sapiens 17 cgccccgggc aggtgtcagg ggttccaaac cagcctgggg aaacacagcg tagacccctc 60 acctctacaa ataaaaaatt aaaaaattag ccaggtgtgg cagcgaacaa ctgtagtctc 120 agatactcag gagactgagc tggaaaggat cacttgagcc caagaagttc aaggttacag 180 tgggccacga tcatgtcatt acactccagc ttgggtgaca aaatgagact gtcta 235 18 2732 DNA Homo sapiens 18 gtgtggagtt tcagctgcta ttgactataa gagctatgga acagaaaaag cttgctggct 60 tcatgttgat aactacttta tatggagctt cattggacct gttaccttca ttattctgct 120 aaatattatc ttcttggtga tcacattgtg caaaatggtg aagcattcaa acactttgaa 180 accagattct agcaggttgg aaaacattaa gtcttgggtg cttggcgctt tcgctcttct 240 gtgtcttctt ggcctcacct ggtcctttgg gttgcttttt attaatgagg agactattgt 300 gatggcatat ctcttcacta tatttaatgc tttccaggga gtgttcattt tcatctttca 360 ctgtgctctc caaaagaaag tacgaaaaga atatggcaag tgcttcagac actcatactg 420 ctgtggaggc ctcccaactg agagtcccca cagttcagtg aaggcatcaa ccaccagaac 480 cagtgctcgc tattcctctg gcacacagag tcgtataaga agaatgtgga atgatactgt 540 gagaaaacaa tcagaatctt cttttatctc aggtgacatc aatagcactt caacacttaa 600 tcaaggtggc ataaatctta atatattatt acaggactga catcacatgg tctgagagcc 660 catcttcaag atttatatca tttagaggac attcactgaa caatgccagg gatacaagtg 720 ccatggatac tctaccgcta aatggtaatt ttaacaacag ctactcgctg cacaagggtg 780 actataatga cagcgtgcaa gttgtggact gtggactaag tctgaatgat actgcttttg 840 agaaaatgat catttcagaa ttagtgcaca acaacttacg gggcagcagc aagactcaca 900 acctcgagct cacgctacca gtcaaacctg tgattggagg tagcagcagt gaagatgatg 960 ctattgtggc agatgcttca tctttaatgc acagcgacaa cccagggctg gagctccatc 1020 acaaagaact cgaggcacca cttattcctc agcggactca ctcccttctg taccaacccc 1080 agaagaaagt gaagtccgag ggaactgaca gctatgtctc ccaactgaca gcagaggctg 1140 aagatcacct acagtccccc aacagagact ctctttatac aagcatgccc aatcttagag 1200 actctcccta tccggagagc agccctgaca tggaagaaga cctctctccc tccaggagga 1260 gtgagaatga ggacatttac tataaaagca tgccaaatct tggagctggc catcagcttc 1320 agatgtgcta ccagatcagc aggggcaata gtgatggtta tataatcccc attaacaaag 1380 aagggtgtat tccagaagga gatgttagag aaggacaaat gcagctggtt acaagtcttt 1440 aatcatacag ctaaggaatt ccaagggcca catgcgagta ttaataaata aagacaccat 1500 tggcctgacg cagctccctc aaactctgct tgaagagatg actcttgacc tgtggttctc 1560 tggtgtaaaa aagatgactg aaccttgcag ttctgtgaat ttttataaaa catacaaaaa 1620 ctttgtatat acacagagta tactaaagtg aattatttgt tacaaagaaa agagatgcca 1680 gccaggtatt ttaagattct gctgctgttt agagaaattg tgaaacaagc aaaacaaaac 1740 tttccagcca ttttactgca gcagtctgtg aactaaattt gtaaatatgg ctgcaccatt 1800 tttgtaggcc tgcattgtat tatatacaag acgtaggctt taaaatcctg tgggacaaat 1860 ttactgtacc ttactattcc tgacaagact tggaaaagca ggagagatat tctgcatcag 1920 tttgcagttc actgcaaatc ttttacatta aggcaaagat tgaaaacatg cttaaccact 1980 agcaatcaag ccacaggcct tatttcatat gtttcctcaa ctgtacaatg aactattctc 2040 atgaaaaatg gctaaagaaa ttatattttg ttctattgct agggtaaaat aaatacattt 2100 gtgtccaact gaaatataat tgtcattaaa ataattttaa agagtgaaga aaatattgtg 2160 aaaagctctt ggttgcacat gttatgaaat gttttttctt acactttgtc atggtaagtt 2220 ctactcattt tcacttcttt tccactgtat acagtgttct gctttgacaa agttagtctt 2280 tattacttac atttaaattt cttattgcca aaagaacgtg ttttatgggg agaaacaaac 2340 tctttgaagc cagttatgtc atgccttgca caaaagtgat gaaatctaga aaagattgtg 2400 tgtcacccct gtttattctt gaacagaggg caaagagggc actgggcact tctcacaaac 2460 tttctagtga acaaaaggtg cctattcttt tttaaaaaaa taaaataaaa cataaatatt 2520 actcttccat attccttctg cctatattta gtaattaatt tattttatga taaagttcta 2580 atgaaatgta aattgtttca gcaaaattct gctttttttt catccctttg tgtaaacctg 2640 ttaataatga gcccatcact aatatccagt gtaaagttta acacggtttg acagtaaata 2700 aatgtgaatt ttttcaagtt aaaaaaaaaa aa 2732 19 276 DNA Homo sapiens 19 ctccctaaat gattttaaaa taaattggat aaacatatga tataaagtgg gtactttaga 60 aaccgccttt gcatattttt tatgtacaaa tctttgtata caattccgat gttccttata 120 tattccctat atagcaaacc aaaaccagga cctcccaact gcatgcctca agtccctgtg 180 gagcactctg gcaactggat ggccctactt gctttctgac aaaatagctg gaaaggagga 240 gggaccaatt aaatacctcg gccgcgacca cgctgg 276 20 2361 DNA Homo sapiens 20 attgtaccag ccttgatgaa cgtgggccct gcttcgcttt tgagggccat aagctcattg 60 cccactggtt tagaggctac cttatcattg tctcccgtga ccggaaggtt tctcccaagt 120 cagagtttac cagcagggat tcacagagct ccgacaagca gattctaaac atctatgacc 180 tgtgcaacaa gttcatagcc tatagcaccg tctttgagga tgtagtggat gtgcttgctg 240 agtggggctc cctgtacgtg ctgacgcggg atgggcgggt ccacgcactg caggagaagg 300 acacacagac caaactggag atgctgttta agaagaacct atttgagatg gcgattaacc 360 ttgccaagag ccagcatctg gacagtgatg ggctggccca gattttcatg cagtatggag 420 accatctcta cagcaagggc aaccacgatg gggctgtcca gcaatatatc cgaaccattg 480 gaaagttgga gccatcctac gtgatccgca agtttctgga tgcccagcgc attcacaacc 540 tgactgccta cctgcagacc ctgcaccgac aatccctggc caatgccgac cataccaccc 600 tgctcctcaa ctgctatacc aagctcaagg acagctcgaa gctggaggag ttcatcaaga 660 aaaagagtga gagtgaagtc cactttgatg tggagacagc catcaaggtc ctccggcagg 720 ctggctacta ctcccatgcc ctgtatctgg cggagaacca tgcacatcat gagtggtacc 780 tgaagatcca gctagaagac attaagaatt atcaggaagc ccttcgatac atcggcaagc 840 tgccttttga gcaggcagag agcaacatga agcgctacgg caagatcctc atgcaccaca 900 taccagagca gacaactcag ttgctgaagg gactttgtac tgattatcgg cccagcctcg 960 aaggccgcag cgatagggag gccccaggct gcagggccaa ctctgaggag ttcatcccca 1020 tctttgccaa taacccgcga gagctgaaag ccttcctaga gcacatgagt gaagtgcagc 1080 cagactcacc ccaggggatc tacgacacac tccttgagct gcgactgcag aactgggccc 1140 acgagaagga tccacaggtc aaagagaagc ttcacgcaga ggccatttcc ctgctgaaga 1200 gtggtcgctt ctgcgacgtc tttgacaagg ccctggtcct gtgccagatg cacgacttcc 1260 aggatggtgt cctttacctt tatgagcagg ggaagctgtt ccagcagatc atgcactacc 1320 acatgcagca cgagcagtac cggcaggtca tcagcgtgtg tgagcgccat ggggagcagg 1380 acccctcctt gtgggagcag gccctcagct acttcgctcg caaggaggag gactgcaagg 1440 agtatgtggc agctgtcctc aagcatatcg agaacaagaa cctcatgcca cctcttctag 1500 tggtgcagac cctggcccac aactccacag ccacactctc cgtcatcagg gactacctgg 1560 tccaaaaact acagaaacag agccagcaga ttgcacagga tgagctgcgg gtgcggcggt 1620 accgagagga gaccacccgt atccgccagg agatccaaga gctcaaggcc agtcctaaga 1680 ttttccaaaa gaccaagtgc agcatctgta acagtgcctt ggagttgccc tcagtccact 1740 tcctgtgtgg ccactccttc caccaacact gctttgagag ttactcggaa agtgatgctg 1800 actgccccac ctgcctccct gaaaaccgga aggtcatgga tatgatccgg gcccaggaac 1860 agaaacgaga tctccatgat caattccagc atcagctcaa gtgctccaat gacagctttt 1920 ctgtgattgc tgactacttt ggcagaggtg ttttcaacaa attgactctg ctgaccgacc 1980 ctcccacagc cagactgacc tccagcctgg aggctgggct gcaacgcgac ctactcatgc 2040 actccaggag gggcacttaa gcagcctgga ggaagatgtg ggcaacagtg gaggaccaag 2100 agaacagaca caatgggacc tgggcgggcg ttacacagaa ggctggctga catgcccagg 2160 gctccactct catctaatgt cacagccctc acaagactaa agcggaactt tttcttttcc 2220 ctggccttcc ttaattttaa gtcaagcttg gcaatccctt cctctttaac taggcaggtg 2280 ttagaatcat ttccagatta atggggggga aggggaacct caggcaaacc tcctgaagtt 2340 ttggaaaaaa aagctggttt c 2361 21 179 DNA Homo sapiens 21 aggtgttaga tgctcttgaa aaagaaactg catctaagct gtcagaaatg gattctttta 60 acaatcaact aaaggaactg agagaaacct acaacacaca gcagttagcc cttgaacagc 120 tttataagat caacgtgaca agttgaagga aattgaaagg aaaaaattag aactaatgc 179 22 905 DNA Homo sapiens 22 tttttttttt ttctttaacc gtgtggtctt tatttcagtg ccagtgttac agatacaaca 60 caaatgttcc agttagaagg aattcaaacg gaatgccaag gtccaagcca ggctcaagaa 120 ataaaaaggg aggtttggag taatagataa gatgactcca atactcactc ttcctaaggg 180 caaaggtact tttgatacag agtctgatct ttgaaactgg tgaactcctc ttccacccat 240 taccatagtt caaacaggca agttatgggc ttaggagcac tttaaaattt gtggtgggaa 300 tagggtcatt aataactatg aatatatctt ttagaaggtg accattttgc actttaaagg 360 gaatcaattt tgaaaatcat ggagactatt catgactaca gctaaagaat ggcgagaaag 420 gggagctgga agagccttgg aagtttctat tacaaataga gcaccatatc cttcatgcca 480 aatctcaaca aaagctcttt ttaactccat ctgtccagtg tttacaaata aactcgcaag 540 gtctgaccag ttcttggtaa caaacataca tgtgtgtgtc tgtgtgtata cagcaatgca 600 cagaaaaggc taccaggagc ctaatgcctc tttcaaacat tgggggaacc agtagaaaaa 660 ggcagggctc cctaatgtcc attattacat ttccattccg aatgccagat gttaaaagtg 720 cctgaagatg gtaacccagc tagtgaggaa taaatacccc accttgccca gtccacagag 780 aaacaacagt agaaagaagg ggcaactctt tgctgcagag acaaagtgag tgttttttcg 840 ccatggattg cagtcctctc ctccagacca gctgcttatt tcctcagggg cccagggaat 900 gttga 905 23 2134 DNA Homo sapiens 23 ggtctcttct ttcctttttt tttttccaaa agtgttcttt tatttctagt aacatatatt 60 gtataaatac tctattttat atgcacttcc acaaaagcga tataatttaa aagttttttt 120 cattagaaat aaatgtataa aaataaatat gttattatag gcatttatta ctaactatag 180 tccttcttgg aaggaacacc caaaccaata cttataaagt acatgtaatt tatagtaaca 240 tattttacta tatacatatg gaaaaaatca tattctcaca gaagagctga acagacattc 300 accaggatac gactgttgga ccagctgctg gagatggacc tgctacccct cagcagcctc 360 cccaccacaa gacaagtgat ctcaatgtcc ccaaacctgt gggaccctgt tctacacacc 420 tcatttttgt tccggcgttt catcctcctt gtgtgattgt actgattttc atgagacaca 480 agttacttct ttacatccat attcccaaag cagggttaca tggtaggaaa gaaaggaagt 540 tggaggtact aagctcattg tgtctcctct agcttttacc agcatctaat gcttcactgc 600 tttttttcca ttgtagactt taatgcactt gaataaatac atggagttgt tttttcctca 660 aaatgaatta cacaaataaa gactgagatg gtccaaaaaa ggaaagagga agccatttgc 720 gttatttcac gttgctgagc ctttctctca tgttgaacaa tctgaagttt taattctcgg 780 tagaaataat gtataaacat tctctgaaac catagcagcc ataaacagtg ctggtcaaag 840 atcctatttg tactcctttc tccccccatt gttagtgagg taaagtaaaa caggtcttag 900 taaaatctca cttttctcct acttttcatt tcccaacccc catgatacta agtatttgat 960 aagtaccagg aaacaggggt tgtaatagtt ctaacttttt ttgacaattg ctttgttttt 1020 tctaaacttg taatagatgt aacaaaagaa ataataataa taatgcccgg ggctttatta 1080 tgctatatca ctgctcagag gttaataatc ctcactaact atcctatcaa atttgcaact 1140 ggcagtttac tctgatgatt caactccttt tctatctacc cccataatcc caccttactg 1200 atacacctca ctggttactg gcaagatacg ctggatccct ccagccttct tgctttccct 1260 gcaccagccc ttcctcactt tgccttgccc tcaaagctaa caccacttaa accacttaac 1320 tgcattctgc cattgtgcaa aagtctatga aatgtttagg tttctttaaa ggatcacagc 1380 tctcatgaga taacacccct ccatcatggg acagacactt caagcttctt tttttgtaac 1440 ccttcccaca ggtcttagaa catgatgacc actcccccag ctgccactgg gggcagggat 1500 ggtctgcaca aggtctggtg ctggctggct tcacttcctt tgcacactcg gaagcaggct 1560 gtccattaat gtctcggcat tctaccagtc ttctctgcca acccaattca catgacttag 1620 aacattcgcc ccactcttca atgacccatg ctgaaaaagt ggggatagca ttgaaagatt 1680 ccttcttctt ctttacgaag taggtgtatt taattttagg tcgaagggca ttgcccacag 1740 taagaacctg gatggtcaag ggctctttga gagggctaaa gctgcgaatt ctttccaatg 1800 ccgcagagga gccgctgtac ctcaagacaa cacctttgta cataatgtct tgctctaagg 1860 tggacaaagt gtagtcacca ttaagaatat atgtgccatc agcagctttg atggcaagaa 1920 agctgccatt gttcctggat cccctctggt tccgctgttt cacttcgatg ttggtggctc 1980 cagttggaat tgtgatgata tcatgatatc caggttttgc actagtaact gatcctgata 2040 tttttttaca agtagatcca tttcccccgc aaacaccaca tttatcaaac ttctttttgg 2100 agtctatgat gcgatcacaa ccagctttta caca 2134 24 1626 DNA Homo sapiens 24 ggacaatttc tagaatctat agtagtatca ggatatattt tgctttaaaa tatattttgg 60 ttattttgaa tacagacatt ggctccaaat tttcatcttt gcacaatagt atgacttttc 120 actagaactt ctcaacattt gggaactttg caaatatgag catcatatgt gttaaggctg 180 tatcatttaa tgctatgaga tacattgttt tctccctatg ccaaacaggt gaacaaacgt 240 agttgttttt tactgatact aaatgttggc tacctgtgat tttatagtat gcacatgtca 300 gaaaaaggca agacaaatgg cctcttgtac tgaatacttc ggcaaactta ttgggtcttc 360 attttctgac agacaggatt tgactcaata tttgtagagc ttgcgtagaa tggattacat 420 ggtagtgatg cactggtaga aatggttttt agttattgac tcagaattca tctcaggatg 480 aatcttttat gtctttttat tgtaagcata tctgaattta ctttataaag atggttttag 540 aaagctttgt ctaaaaattt ggcctaggaa tggtaacttc attttcagtt gccaaggggt 600 agaaaaataa tatgtgtgtt gttatgttta tgttaacata ttattaggta ctatctatga 660 atgtatttaa atatttttca tattctgtga caagcattta taatttgcaa caagtggagt 720 ccatttagcc cagtgggaaa gtcttggaac tcaggttacc cttgaaggat atgctggcag 780 ccatctcttt gatctgtgct taaactgtaa tttatagacc agctaaatcc ctaacttgga 840 tctggaatgc attagttatg ccttgtacca ttcccagaat ttcaggggca tcgtgggttt 900 ggtctagtga ttgaaaacac aagaacagag agatccagct gaaaaagagt gatcctcaat 960 atcctaacta actggtcctc aactcaagca gagtttcttc actctggcac tgtgatcatg 1020 aaacttagta gaggggattg tgtgtatttt atacaaattt aatacaatgt cttacattga 1080 taaaattctt aaagagcaaa actgcatttt atttctgcat ccacattcca atcatattag 1140 aactaagata tttatctatg aagatataaa tggtgcagag agactttcat ctgtggattg 1200 cgttgtttct tagggttcct agcactgatg cctgcacaag catgtgatat gtgaaataaa 1260 atggattctt ctatagctaa atgagttccc tctggggaga gttctggtac tgcaatcaca 1320 atgccagatg gtgtttatgg gctatttgtg taagtaagtg gtaagatgct atgaagtaag 1380 tgtgtttgtt ttcatcttat ggaaactctt gatgcatgtg cttttgtatg gaataaattt 1440 tggtgcaata tgatgtcatt caactttgca ttgaattgaa ttttggttgt atttatatgt 1500 attatacctg tcacgcttct agttgcttca accattttat aaccattttt gtacatattt 1560 tacttgaaaa tattttaaat ggaaatttaa ataaacattt gatagtttac ataataaaaa 1620 aaaaaa 1626 25 1420 DNA Homo sapiens 25 gttcagcatt gtttctgctt ctgaaatctg tatagtacac tggtttgtaa tcattatgtc 60 ttcattgaaa tccttgctac ttctcttcct cctcaatgaa agacacgaga gacaagagcg 120 acacaagctt aagaaaaacg agcaaggaag agtatcttca ttattctcat tttctctgag 180 ttggaaacaa aaacatgaag gactccaact agaagacaga tatttacatt taaatagatt 240 agtgggaaaa ctttaagagt ttccacatat tagttttcat tttttgagtc aagagactgc 300 tccttgtact gggagacact agtagtatat gtttgtaatg ttactttaaa attatctttt 360 tattttataa ggcccataaa tactggttaa actctgttaa aagtgggcct tctatcttgg 420 atggtttcac tgccatcagc catgctgata tattagaaat ggcatcccta tctacttact 480 ttaatgctta aaattataca taaaatgctt tatttagaaa acctacatga tacagtggtg 540 tcagccttgc catgtatcag tttcacttga aatttgagac caattaaatt tcaactgttt 600 agggtggaga aagaggtact ggaaaacatg cagatgagga tatcttttat gtgcaacagt 660 atcctttgca tgggaggaga gttactcttg aaaggcaggc agcttaagtg gacaatgttt 720 tgtatatagt tgagaatttt acgacacttt taaaaattgt gtaattgtta aatgtccagt 780 tttgctctgt tttgcctgaa gttttagtat ttgttttcta ggtggacctc tgaaaaccaa 840 accagtacct ggggaggtta gatgtgtgtt tcaggcttgg agtgtatgag tggttttgct 900 tgtattttcc tccagagatt ttgaacttta ataattgcgt gtgtgttttt ttttttttaa 960 gtggctttgt ttttttttct caagtaaaat tgtgaacata tttcctttat aggggcaggg 1020 catgagttag ggagactgaa gagtattgta gactgtacat gtgccttctt aatgtgtttc 1080 tcgacacatt ttttttcagt aacttgaaaa ttcaaaaggg acatttggtt aggttactgt 1140 acatcaatct atgcataaat ggcagcttgt tttcttgagc cactgtctaa attttgtttt 1200 tatagaaatt ttttatactg attggttcat agatggtcag ttttgtacac agactgaaca 1260 atacagcact ttgccaaaaa tgagtgtagc attgtttaaa cattgtgtgt taacacctgt 1320 tctttgtaat tgggttgtgg tgcattttgc actacctgga gttacagttt tcaatctgtc 1380 agtaaataaa gtgtccttta acttcaaaaa aaaaaaaaaa 1420 26 689 DNA Homo sapiens 26 aaacaaacaa aaaaaaagtt agtactgtat atgtaaatac tagcttttca atgtgctata 60 caaacaatta tagcacatcc ttccttttac tctgtctcac ctcctttagg tgagtacttc 120 cttaaataag tgctaaacat acatatacgg aacttgaaag ctttggttag ccttgcctta 180 ggtaatcagc ctagtttaca ctgtttccag ggagtagttg aattactata aaccattagc 240 cacttgtctc tgcaccattt atcacaccag gacagggtct ctcaacctgg gcgctactgt 300 catttggggc caggtgattc ttccttgcaa gggctgtcct gtacctgccc gggcggccgc 360 tcgaagcgtg gtcgcggccg aggtactgaa aggaccaagg agctctggct gccctcagga 420 attccaaatg accgaaggaa caaagcttca gggctctggg tggtgtctcc cactattcag 480 gaggtggtcg gaggtaacgc agcttcattt cgtccagtcc tttccagtat ttaaagttgt 540 tgtcaagatg ctgcattaaa tcaggcaggt ctacaaaggc atcccaagca tcaaacatgt 600 ctgtgatgaa gtaatcaatg aaacaccgga acctccgacc acctcctgaa tagtgggaga 660 cacacccaga gcctgaagtt tgtccttcg 689 27 471 DNA Homo sapiens 27 tcccagcggc atgaagtttg agattggcca ggccctgtac ctgggcttca tctccttcgt 60 ccctctcgct cattggtggc accctgcttt gcctgtcctg ccaggacgag gcaccctaca 120 agccctaacc caggccccgc ccagggccac cacgaccact gcaaacaccg cacctgccta 180 ccagccacca gctgcctaca aagacaatcg ggccccctca gtgacctcgg ccaccacagc 240 gggtacaggc tgaacgacta cgtgtgagtc cccacagcct gcttctcccc tgggctgctg 300 tgggctggtt cccggcggga ctgtcaatgg aggcaggggt tccagcacaa agtttacttc 360 tgggcaattt ttgtatccaa ggaaataatg tgaatgcgag gaaatgtctt tagagcacag 420 ggacagaggg ggaaataaga ggaggagaaa gctctctata ccaaagactg a 471 28 929 DNA Homo sapiens 28 ggtgaactca gtgcattggg ccaatggttc gacacaggct ctgccagcca caaccatcct 60 gctgcttctg acggtttggc tgctggtggg ctttcccctc actgtcattg gaggcatctt 120 tgggaagaac aacgccagcc cctttgatgc accctgtcgc accaagaaca tcgcccggga 180 gattccaccc cagccctggt acaagtctac tgtcatccac atgactgttg gaggcttcct 240 gcctttcagt gccatctctg tggagctgta ctacatcttt gccacagtat ggggtcggga 300 gcagtacact ttgtacggca tcctcttctt tgtcttcgcc atcctgctga gtgtgggggc 360 ttgcatctcc attgcactca cctacttcca gttgtctggg gaggattacc gctggtggtg 420 gcgatctgtg ctgagtgttg gctccaccgg cctcttcatc ttcctctact cagttttcta 480 ttatgcccgg cgctccaaca tgtctggggc agtacagaca gtagagttct tcggctactc 540 cttactcact ggttatgtct tcttcctcat gctgggcacc atctcctttt tttcttccct 600 aaagttcatc cggtatatct atgttaacct caagatggac tgagttctgt atggcagaac 660 tattgctgtt ctctcccttt cttcatgccc tgttgaactc tcctaccagc ttctcttctg 720 attgactgaa ttgtgtgatg gcattgttgc cttccctttt tccctttggg cattccttcc 780 ccagagaggg cctggaaatt ataaatctct atcacataag gattatatat ttgaactttt 840 taagttgcct ttagttttgg tcctgatttt tctttttaca attaccaaaa taaaatttat 900 taagaaaaag aaaaaaaaaa aaaaaaaaa 929 29 1775 DNA Homo sapiens 29 gaacgtgatg ggaactttgg gaggatgtct gagaaaatgt ccgaagggat tttggccaac 60 accagaaaac gccaatgtcc taggaattcc ctcccaaaat gcttcccaaa aaattactca 120 ttgacaattc aaattgcact tggctggcgg cagcccgggc ggccttcagt ccgtgtgggg 180 cgcccgcgtg gccttctcct cgtaggactc cccaaactcg ttcactctgc gtttatccac 240 aggataaagc caccgctggt acaggtagac cagaaacacc acgtcgtccc ggaagcaggc 300 cagccggtga gacgtgggca tggtgatgat gaaggcaaag acgtcatcaa tgaaggtgtt 360 gaaagccttg taggtgaagg ccttccaggg cagatgtgcc actgacttca acttgtagtt 420 cacaaagagc tggggcagca tgaagaggaa accaaaggca tagaccccgt tgacgaagct 480 gttgattaac caggagtacc agctcttata tttgatattc aggagtgaat agacagcacc 540 cccgacacag agagggtaca gcaggtatga caagtacttc atggcctgag tatcgtactc 600 ctcggttttc ctctcagatt cgctgtaagt gccaaactga aattcgggca tcaggcctct 660 ccaaaaaata gtcatcttca atgccttctt cactttccac agctcaatgg cggctccaac 720 acccgccggg accagcacca gcaggctcgt ctgctcgtcc agcaggaaca gaaagatgac 780 cacggtgctg aagcagcgcc agagcactgc cttggtggac atgccgatca tgctcttctt 840 cttcttccag aaactgatgt catttttaaa ggccaggaaa tcaaagagaa gatggaacgc 900 tgcgacaaag aaggtcagcg ccaggaagta taagttggta tctacaaaaa ttcctttcac 960 ctcatcagca tctttctctg aaaacccgaa ctgctgcagg gagtacacgg cgtcctgcat 1020 gtggatccag aagcgcagcc gccccagtga gaccttgtcg taggacacgg tgaggggcag 1080 ctcggtggtg gagcggttta tgaccatcag gtccttcacg cggttgctga gctggtcgat 1140 gaacaggatg ggcaggtaat gcacggtttt ccccagctgg atcatcttca tgtaccgatg 1200 cacatcggca ggcagggagg acccgtcaaa gacaaagttg tccgccatca cgttcagcgc 1260 cagccgcggt cgccagtggg acactggctc atccagggca ctcgtcggct tcttctccgc 1320 ctcgatctgc tgtgtatcag actccccggt gagcaggttg atttcttctg gcttggggac 1380 catgtaggtg gtcagaggac tgaccaggtg cacctgcttc ccgtcgtgcc acggcaggac 1440 cccagcgtga tggaggaaga tgtaggcata cagcgtccca ttgtttctcg ttttctttgg 1500 tacagaaaca ttaactgtcc tttcaaattt ggactccaca tcaaagtctt ccacattcaa 1560 gaccaggtcg atgttgttct cagcacccag gtgggacctc gtcgtggtgt acacgctcag 1620 ctgcagcttg ggccgccgcg ccaggtaggg ctggatgcag ttggcgtcgc cggagcacgg 1680 gcgggtgtag acgatgccgt acatgaccca gcaggtgtgc accacgtaga ccacgaacac 1740 gcccaccacc aagctggtga aggagctgcg gcccc 1775 30 1546 DNA Homo sapiens 30 aaaataagta ggaatgggca gtgggtattc acattcacta caccttttcc atttgctaat 60 aaggccctgc caggctggga gggaattgtc cctgcctgct tctggagaaa gaagatattg 120 acaccatcta cgggcaccat ggaactgctt caagtgacca ttctttttct tctgcccagt 180 atttgcagca gtaacagcac aggtgtttta gaggcagcta ataattcact tgttgttact 240 acaacaaaac catctataac aacaccaaac acagaatcat tacagaaaaa tgttgtcaca 300 ccaacaactg gaacaactcc taaaggaaca atcaccaatg aattacttaa aatgtctctg 360 atgtcaacag ctactttttt aacaagtaaa gatgaaggat tgaaagccac aaccactgat 420 gtcaggaaga atgactccat catttcaaac gtaacagtaa caagtgttac acttccaaat 480 gctgtttcaa cattacaaag ttccaaaccc aagactgaaa ctcagagttc aattaaaaca 540 acagaaatac caggtagtgt tctacaacca gatgcatcac cttctaaaac tggtacatta 600 acctcaatac cagttacaat tccagaaaac acctcacagt ctcaagtaat aggcactgag 660 ggtggaaaaa atgcaagcac ttcagcaacc agccggtctt attccagtat tattttgccg 720 gtggttattg ctttgattgt aataacactt tcagtatttg ttctggtggg tttgtaccga 780 atgtgctgga aggcagatcc gggcacacca gaaaatggaa atgatcaacc tcagtctgat 840 aaagagagcg tgaagcttct taccgttaag acaatttctc atgagtctgg tgagcactct 900 gcacaaggaa aaaccaagaa ctgacagctt gaggaattct ctccacacct aggcaataat 960 tacgcttaat cttcagcttc tatgcaccaa gcgtggaaaa ggagaaagtc ctgcagaatc 1020 aatcccgact tccatacctg ctgctggact gtaccagacg tctgtcccag taaagtgatg 1080 tccagctgac atgcaataat ttgatggaat caaaaagaac cccggggctc tcctgttctc 1140 tcacatttaa aaattccatt actccattta caggagcgtt cctaggaaaa ggaattttag 1200 gaggagaatt tgtgagcagt gaatctgaca gcccaggagg tgggctcgct gataggcatg 1260 actttcctta atgtttaaag ttttccgggc caagaatttt tatccatgaa gactttccta 1320 cttttctcgg tgttcttata ttacctactg ttagtattta ttgtttacca ctatgttaat 1380 gcagggaaaa gttgcacgtg tattattaaa tattaggtag aaatcatacc atgctacttt 1440 gtacatataa gtattttatt cctgctttcg tgttactttt aataaataac tactgtactc 1500 aatactctaa aaatactata acatgactgt gaaaatggca aaaaaa 1546 31 750 DNA Homo sapiens 31 cacttgggca cccccatttt ctaaaaaaat ggaaatctgg agggcaaaaa aggtgtgctg 60 aagggaagtg cctctgatgg cccaaaaacc ttcttccaaa ctagtgtagg aatggaatgg 120 atagcaaatg gatccttttt ggcctccttt ggagcatgcc ttccctatct tatccttggc 180 cccactaaag cagaacgtta cggatatttc tgtttttgcc attggatgcc tatctggcca 240 aacagccttt ccctaattgg aaaatgcagt cctgtttaaa acctttgatt tacgactact 300 tgtacatgct tgctcattac aattttgaca ttttttacat agtgaagacc ccaaacatat 360 cagtgaaaca tgacaagatc ataaagaaca gtatcatatt attatttagt cgcttttaca 420 gtggcaagcc aattttgaaa tatctcattt aaaactcaga cccaattcac tgagttatac 480 ttttaatagc ttcctcagca cactatttcc catgcattaa atatgataaa ataatctatc 540 actgcccatc ggtcttgtaa aaaggaagtc tgaatacaga gcccacaaca ctaaaattgt 600 ttttctagct acaaagtata gcatcatcaa cacagacacg atttggactc cctgacaggt 660 ggattggaaa acggtgttta aagagaagag aacattttaa cataaatgtc attaagaatc 720 ccaaaggcct tatttgtcac caccgtcccg 750 32 1620 DNA Homo sapiens 32 gcaattcccc cctcccacta aacgactccc agtaattatg tttacaaccc attggatgca 60 gtgcagccat tcataagaac cttggtgccc cagaaaaatc tgtccttttt ggtaccaaac 120 ctgaggtctt ttggaagata atgtagaaaa ccactaccta ttgaaggcct gttttggcta 180 atctgtgcaa actctgatga tacctgcctt atgtggattc ttttccacac tgctttcatt 240 tttaagtata aagacttaga aaactagaat aatgctttta caaataatta aaagtatgtg 300 atgttctggg ttttttcctt ctttttagaa ccccgcctcc atttaaaaaa ttaaaaaaaa 360 aaaaaaaact tttaacattt aaaaaataaa aattaacaaa atttcactta ttccaggaca 420 cgctggcatt tggactcaat gaaaagggca cctaaagaaa ataaggctga ctgaatgttt 480 tccataattt tcacacaata acagtccctt tctatccagc ttgccttcca tttatctcta 540 gggttagctt ttcaggcaac atccttggtc attgcccaga aagtacctga gctatcagtg 600 attggaatgg cacaggaaac cgaatcacat gggtgccctc cccttggttt tcaagtatct 660 tggagttgtg cacaaaaatt aggtcatgcc ttcagtgtct tgttctttaa acctaccctt 720 tgacaatcag gtgctaatga ttgtatacta ttaaaaccag cacataagta ttgtaaatgt 780 gtgttcctcc taggttggaa gaaatgtctt tccttctatc tgggtcctgt taaagcgggt 840 gtcagttgtg tcttttcacc tcgatttgtg aattaataga attgggggga gaggaaatga 900 tgatgtcaat taagtttcag gtttggcatg atcatcattc tcgatgatat tctcactttg 960 tcgcaaatct gcccttatcg taagaacaag tttcagaatt ttccctccac tatacgactc 1020 cagtattatg tttacaatcc attggatgag tgcagcatta taagaccttg gtgcccagaa 1080 aaatctgtcc tttttggtac caaacctgag gtcttttgga agataatgta gaaaaccact 1140 acctattgaa ggcctgtttt ggctaatctg tgcaaactct gatgatacct gcttatgtgg 1200 attcttttcc acactgcttt catttttaag tataaagact tagaaaacta gaataatgct 1260 tttacaaata attaaaagta tgtgatgttc tgggtttttt ccttcttttt agaaccctgt 1320 atttaaacaa gccttctttt taagtcttgt ttgaaattta agtctcagat cttctggata 1380 ccaaatcaaa aacccaacgc gtaaaacagg gcagtatttg tgttcctaat tttaaaaagc 1440 tttatgtata ctctataaat atagatgcat aaacaacact tccccttgag tagcacatca 1500 acatacagca ttgtacatta caatgaaaat gtgtaactta agggtattat atatataaat 1560 acatatatac ctttgtaacc tttatactgt aaataaaaaa gttgctttag tcaaaaaaaa 1620 33 2968 DNA Homo sapiens 33 gaaaaagtag aaggaaacac agttcatata gaagtaaaag aaaaccctga agaggaggag 60 gaggaggaag aagaggaaga agaagatgaa gaaagtgaag aggaggagga agaggaggga 120 gaaagtgaag gcagtgaagg tgatgaggaa gatgaaaagg tgtcagatga gaaggattca 180 gggaagacat tagataaaaa gccaagtaaa gaaatgagct cagattctga atatgactct 240 gatgatgatc ggactaaaga agaaagggct tatgacaaag caaaacggag gattgagaaa 300 cggcgacttg aacatagtaa aaatgtaaac accgaaaagc taagagcccc tattatctgc 360 gtacttgggc atgtggacac agggaagaca aaaattctag ataagctccg tcacacacat 420 gtacaagatg gtgaagcagg tggtatcaca caacaaattg gggccaccaa tgttcctctt 480 gaagctatta atgaacagac taagatgatt aaaaattttg atagagagaa tgtacggatt 540 ccaggaatgc taattattga tactcctggg catgaatctt tcagtaatct gagaaataga 600 ggaagctctc tttgtgacat tgccatttta gttgttgata ttatgcatgg tttggagccc 660 cagacaattg agtctatcaa ccttctcaaa tctaaaaaat gtcccttcat tgttgcactc 720 aataagattg ataggttata tgattggaaa aagagtcctg actctgatgt ggctgctact 780 ttaaagaagc agaaaaagaa tacaaaagat gaatttgagg agcgagcaaa ggctattatt 840 gtagaatttg cacagcaggg tttgaatgct gctttgtttt atgagaataa agatccccgc 900 acttttgtgt ctttggtacc tacctctgca catactggtg atggcatggg aagtctgatc 960 taccttcttg tagagttaac tcagaccatg ttgagcaaga gacttgcaca ctgtgaagag 1020 ctgagagcac aggtgatgga ggttaaagct ctcccgggga tgggcaccac tatagatgtc 1080 atcttgatca atgggcgttt gaaggaagga gatacaatca ttgttcctgg agtagaaggg 1140 cccattgtaa ctcagattcg aggcctcctg ttacctcctc ctatgaagga attacgagtg 1200 aagaaccagt atgaaaagca taaagaagta gaagcagctc agggggtaaa gattcttgga 1260 aaagacctgg agaaaacatt ggctggttta cccctccttg tggcttataa agaagatgaa 1320 atccctgttc ttaaagatga attgatccat gagttaaagc agacactaaa tgctatcaaa 1380 ttagaagaaa aaggagtcta tgtccaggca tctacactgg gttctttgga agctctactg 1440 gaatttctga aaacatcaga agtgccctat gcaggaatta acattggccc agtgcataaa 1500 aaagatgtta tgaaggcttc agtgatgttg gaacatgacc ctcagtatgc agtaattttg 1560 gccttcgatg tgagaattga acgagatgca caagaaatgg ctgatagttt aggagttaga 1620 atttttagtg cagaaattat ttatcattta tttgatgcct ttacaaaata tagacaagac 1680 tacaagaaac agaaacaaga agaatttaag cacatagcag tatttccctg caagataaaa 1740 atcctccctc agtacatttt taattctcga gatccgatag tgatgggggt gacggtggaa 1800 gcaggtcagg tgaaacaggg gacacccatg tgtgtcccaa gcaaaaattt tgttgacatc 1860 ggaatagtaa caagtattga aataaaccat aaacaagtgg atgttgcaaa aaaaggacaa 1920 gaagtttgtg taaaaataga acctatccct ggtgagtcac ccaaaatgtt tggaagacat 1980 tttgaagcta cagatattct tgttagtaag atcagccggc agtccattga tgcactcaaa 2040 gactggttca gagatgaaat gcagaagagt gactggcagc ttattgtgga gctgaagaaa 2100 gtatttgaaa tcatctaatt ttttcacatg gagcaggaac tggagtaaat gcaatactgt 2160 gttgtaatat cccaacaaaa atcagacaaa aaatggaaca gacgtatttg gacactgatg 2220 gacttaagta tggaaggaag aaaaataggt gtataaaatg ttttccatga gaaaccaaga 2280 aacttacact ggtttgacag tggtcagtta catgtcccca cagttccaat gtgcctgttc 2340 actcacctct cccttcccca acccttctct acttggctgc tgttttaaag tttgcccttc 2400 cccaaatttg gatttttatt acagatctaa agctctttcg attttatact gattaaatca 2460 gtactgcagt atttgattaa aaaaaaaaaa gcagattttg tgattcttgg gacttttttg 2520 acgtaagaaa tacttcttta tttatgcata ttcttcccac agtgattttt ccagcattct 2580 tctgccatat gcctttaggg cttttataaa atagaaaatt aggcattctg atatttcttt 2640 agctgctttg tgtgaaacca tggtgtaaaa gcacagctgg ctgcttttta ctgcttgtgt 2700 agtcacgagt ccattgtaat catcacaatt ctaaaccaaa ctaccaataa agaaaacaga 2760 catccaccag taagcaagct ctgttaggct tccatggtta gtggtagctt ctctcccaca 2820 agttgtcctc ctaggacaag gaattatctt aacaaactaa actatccatc acactacctt 2880 ggtatgccag cacctgggta acagtaggag attttataca ttaatctgat ctgtttaatc 2940 tgatcggttt agtagagatt ttatacat 2968 34 6011 DNA Homo sapiens 34 acggggcgcc ggacgacccg cacatcttat cctccacgcc ccactcgcac tcggagcggg 60 accgccccgg actccccctc gggccggcca ctcgaggagt gaggagagag gccgccggcc 120 cggcttgagc cgagcgcagc accccccgcg ccccgcgcca gaagtttggt tgaaccgggc 180 tgccgggaga aacttttttc ttttttcccc ctctcccggg agagtctctg gaggaggagg 240 ggaactcccc cggcccaagg ctcgtgggct cggggtcgcg cggccgcaga aggggcgggg 300 tccgcccgcg aggggaggcg cccccgggga cccgagaggg gggtgaggac cgcgggctgc 360 tggtgcggcg gcggcagcgt gtgccccgcg caggggaggc gccgccccgc tcccggcccg 420 gctgcgagga ggaggcggcg gcggcgcagg aggatgtact tggtggcggg ggacaggggg 480 ttggccggct gcgggcacct cctggtctcg ctgctggggc tgctgctgct gccggcgcgc 540 tccggcaccc gggcgctggt ctgcctgccc tgtgacgagt ccaagtgcga ggagcccagg 600 aaccgcccgg ggagcatcgt gcagggcgtc tgcggctgct gctacacgtg cgccagccag 660 gggaacgaga gctgcggcgg caccttcggg atttacggaa cctgcgaccg ggggctgcgt 720 tgtgtcatcc gccccccgct caatggcgac tccctcaccg agtacgaagc gggcgtttgc 780 gaagatgaga actggactga tgaccaactg cttggtttta aaccatgcaa tgaaaacctt 840 attgctggct gcaatataat caatgggaaa tgtgaatgta acaccattcg aacctgcagc 900 aatccctttg agtttccaag tcaggatatg tgcctttcag ctttaaagag aattgaagaa 960 gagaagccag attgctccaa ggcccgctgt gaagtccagt tctctccacg ttgtcctgaa 1020 gattctgttc tgatcgaggg ttatgctcct cctggggagt gctgtccctt acccagccgc 1080 tgcgtgtgca accccgcagg ctgtctgcgc aaagtctgcc agccgggaaa cctgaacata 1140 ctagtgtcaa aagcctcagg gaagccggga gagtgctgtg acctctatga gtgcaaacca 1200 gttttcggcg tggactgcag gactgtggaa tgccctactg ttcagcagac cgcgtgtccc 1260 ccggacagct atgaaactca agtcagacta actgcagatg gttgctgtac tttgccaaca 1320 agatgcgagt gtctctctgg cttatgtggt ttccccgtgt gtgaggtggg atccactccc 1380 cgcatagtct ctcgtggcga tgggacacct ggaaagtgct gtgatgtctt tgaatgtgtt 1440 aatgatacaa agccagcctg cgtatttaac aatgtggaat attatgatgg agacatgttt 1500 cgaatggaca actgtcggtt ctgtcgatgc caagggggcg ttgccatctg cttcaccgcc 1560 cagtgtggtg agataaactg cgagaggtac tacgtgcccg aaggagagtg ctgcccagtg 1620 tgtgaagatc cagtgtatcc ttttaataat cccgctggct gctatgccaa tggcctgatc 1680 cttgcccacg gagaccggtg gcgggaagac gactgcacat tctgccagtg cgtcaacggt 1740 gaacgccact gcgttgcgac cgtctgcgga cagacctgca caaaccctgt gaaagtgcct 1800 ggggagtgtt gccctgtgtg cgaagaacca accatcatca cagttgatcc acctgcatgt 1860 ggggagttat caaactgcac tctgacacgg aaggactgca ttaatggttt caaacgcgat 1920 cacaatggtt gtcggacctg tcagtgcata aacacccagg aactatgttc agaacgtaaa 1980 caaggctgca ccttgaactg tcccttcggt ttccttactg atgcccaaaa ctgtgagatc 2040 tgtgagtgcc gcccaaggcc caagaagtgc agacccataa tctgtgacaa gtattgtcca 2100 cttggattgc tgaagaataa gcacggctgt gacatctgtc gctgtaagaa atgtccagag 2160 ctctcatgca gtaagatctg ccccttgggt ttccagcagg acagtcacgg ctgtcttatc 2220 tgcaagtgca gagaggcctc tgcttcagct gggccaccca tcctgtcggg cacttgtctc 2280 accgtggatg gtcatcatca taaaaatgag gagagctggc acgatgggtg ccgggaatgc 2340 tactgtctca atggacggga aatgtgtgcc ctgatcacct gcccggtgcc tgcctgtggc 2400 aaccccacca ttcaccctgg acagtgctgc ccatcatgtg cagatgactt tgtggtgcag 2460 aagccagagc tcagtactcc ctccatttgc cacgcccctg gaggagaata ctttgtggaa 2520 ggagaaacgt ggaacattga ctcctgtact cagtgcacct gccacagcgg acgggtgctg 2580 tgtgagacag aggtgtgccc accgctgctc tgccagaacc cctcacgcac ccaggattcc 2640 tgctgcccac agtgtacaga tcaacctttt cggccttcct tgtcccgcaa taacagcgta 2700 cctaattact gcaaaaatga tgaaggggat atattcctgg cagctgagtc ctggaagcct 2760 gacgtttgta ccagctgcat ctgcattgat agcgtaatta gctgtttctc tgagtcctgc 2820 ccttctgtat cctgtgaaag acctgtcttg agaaaaggcc agtgttgtcc ctactgcata 2880 aaagacacaa ttccaaagaa ggtggtgtgc cacttcagtg ggaaggccta tgccgacgag 2940 gagcggtggg accttgacag ctgcacccac tgctactgcc tgcagggcca gaccctctgc 3000 tcgaccgtca gctgcccccc tctgccctgt gttgagccca tcaacgtgga aggaagttgc 3060 tgcccaatgt gtccagaaat gtatgtccca gaaccaacca atatacccat tgagaagaca 3120 aaccatcgag gagaggttga cctggaggtt cccctgtggc ccacgcctag tgaaaatgat 3180 atcgtccatc tccctagaga tatgggtcac ctccaggtag attacagaga taacaggctg 3240 cacccaagtg aagattcttc actggactcc attgcctcag ttgtggttcc cataattata 3300 tgcctctcta ttataatagc attcctattc atcaatcaga agaaacagtg gataccactg 3360 ctttgctggt atcgaacacc aactaagcct tcttccttaa ataatcagct agtatctgtg 3420 gactgcaaga aaggaaccag agtccaggtg gacagttccc agagaatgct aagaattgca 3480 gaaccagatg caagattcag tggcttctac agcatgcaaa aacagaacca tctacaggca 3540 gacaatttct accaaacagt gtgaagaaag gcaactagga tgaggtttca aaagacggaa 3600 gacgactaaa tctgctctaa aaagtaaact agaatttgtg cacttgctta gtggattgta 3660 ttggattgtg acttgatgta cagcgctaag accttactgg gatgggctct gtctacagca 3720 atgtgcagaa caagcattcc cacttttcct caagataact gaccaagtgt tttcttagaa 3780 ccaaagtttt taaagttgct aagatatatt tgcctgtaag atagctgtag agatatttgg 3840 ggtggggaca gtgagtttgg atggggaaag gggtgggagg gtggtgttgg gaagaaaaat 3900 tggtcagctt ggctcgggga gaaacctggt aacataaaag cagttcagtg gcccagaggt 3960 tatttttttc ctattgctct gaagactgca ctggttgctg caaagctcag gcctgaatga 4020 gcaggaaaca aaaaaggcct tgcgacccag ctgccataac caccttagaa ctaccagacg 4080 agcacatcag aaccctttga cagccatccc aggtctaaag ccacaagttt cttttctata 4140 cagtcacaac tgcagtaggc agtgaggaag ccagagaaat gcgatagcgg catttctcta 4200 aagcgggtta ttaaggatat atacagttac actttttgct gcttttattt tcttccaagc 4260 caatcaatca gccagttcct agcagagtca gcacatgaac aagatctaag tcatttcttg 4320 atgtgagcac tggagctttt tttttttaca acgtgacagg aagaggaggg agagggtgac 4380 gaacaccagg catttccagg ggctatattt cactgtttgt tgttgctttg ttctgttata 4440 ttgttggttg ttcatagttt ttgttgaagc tctagcttaa gaagaaactt tttttaaaaa 4500 gactgtttgg ggattctttt tccttattat atactgattc tacaaaatag aaactacttc 4560 attttaattg tatattattc aagcaccttt gttgaagctc aaaaaaaatg atgcctcttt 4620 aaactttagc aattatagga gtatttatgt aactatctta tgcttcaaaa aacaaaagta 4680 tttgtgtgca tgtgtatata atatatatat atacatatat atttatacac atacaattta 4740 tgttttcctg ttgaatgtat ttttatgaga ttttaaccag aacaaaggca gataaacagg 4800 cattccatag cagtgctttt gatcacttac aaattttttg aataacacaa aatctcattc 4860 tacctgcagt ttaattggaa agatgtgtgt gtgagagtat gtatgtgtgt gtgtgtgtgt 4920 gtgtgtgcgc gcgcacgcac gccttgagca gtcagcattg cacctgctat ggagaagggt 4980 attcctttat taaaatcttc ctcatttgga tttgctttca gttggttttc aatttgctca 5040 ctggccagag acattgatgg cagttcttat ctgcatcact aatcagctcc tggatttttt 5100 tttttttttt tcaaacaatg gtttgaaaca actactggaa tattgtccac aataagctgg 5160 aagtttgttg tagtatgcct caaatataac tgactgtata ctatagtggt aacttttcaa 5220 acagccctta gcacttttat actaattaac ccatttgtgc attgagtttt cttttaaaaa 5280 tgcttgttgt gaaagacaca gatacccagt atgcttaacg tgaaaagaaa atgtgttctg 5340 ttttgtaaag gaactttcaa gtattgttgt aaatacttgg acagaggttg ctgaacttta 5400 aaaaaaatta atttattatt ataatgacct aatttattaa tctgaagatt aaccattttt 5460 ttgtcttaga atatcaaaaa gaaaaagaaa aaggtgttct agctgtttgc atcaaaggaa 5520 aaaaagattt attatcaagg ggcaatattt ttatcttttc caaaataaat ttgttaatga 5580 tacattacaa aaatagattg acatcagcct gattagtata aattttgttg gtaattaatc 5640 cattcctggc ataaaaagtc tttatcaaaa aaaattgtag atgcttgctt tttgtttttt 5700 caatcatggc catattatga aaatactaac aggatatagg acaaggtgta aattttttta 5760 ttattatttt aaagatatga tttatcctga gtgctgtatc tattactctt ttactttggt 5820 tcctgttgtg ctcttgtaaa agaaaaatat aatttcctga agaataaaat agatatatgg 5880 cacttggagt gcatcatagt tctacagttt gtttttgttt tcttcaaaaa agctgtaaga 5940 gaattatctg caacttgatt cttggcagga aataaacatt ttgagttgaa atcaaaaaaa 6000 aaaaaaaaaa a 6011 35 716 DNA Homo sapiens 35 gcagtacctg gagtgtcctg cagggggaaa gcgaaccggg ccctgaagtc cggggcagtc 60 acccggggct cctgggccgc tctgccgggc tggggctgag cagcgatcct gctttgtccc 120 agaagtccag agggatcagc cccagaacac accctcctcc ccgggacgcc gcagctttct 180 ggaggctgag gaaggcatga agagtgggct ccacctgctg gccgactgag aaaagaattt 240 ccagaactcg gtcctatttt acagattgag aaactatggt tcaagaagag aggacggggc 300 ttgagggaat ctcctgattc tccttatatg acctcaaact gaccatacta aacagtgtag 360 aaggtctttt taaggctcta aatgtcaggg tctcccatcc cctgatgcct gacttgtaca 420 gtcagtgtgg agtagacggt ttcctccacc cagggttgac tcagggggat gatctgggtc 480 ccattctggt cttaagaccc caaacaaggg ttttttcagc tccaggatct ggagcctcta 540 tctggttagt gtcgtaacct ctgtgtgcct cccgttaccc catctgtcca gtgagctcag 600 cccccatcca cctaacaggg tggccacagg gattactgag ggttaagacc ttagaactgg 660 gtctagcacc cgataagagc tcaataaatg ttgttccttt ccacatcaaa aaaaaa 716 36 395 DNA Homo sapiens 36 ccaatacttc attcttcatt ggtggagaag attgtagact tctaagcatt ttccaaataa 60 aaaagctatg atttgatttc caacttttaa acattgcatg tcctttgcca tttactacat 120 tctccaaaaa aaccttgaaa tgaagaaggc cacccttaaa atacttcaga ggctgaaaat 180 atgattatta cattggaatc ctttagccta tgtgatattt ctttaacttt gcactttcac 240 gcccagtaaa accaaagtca gggtaaccaa tgtcatttta caaaatgtta aaaccctaat 300 tgcagttcct tttttaaatt attttaaaga ttacttaaca acattagaca gtgcaaaaaa 360 agaagcaagg aaagcattct taattctacc atcct 395 37 134 DNA Homo sapiens 37 ccctcgagcg gccgcccggg caggtacttt taccaccgaa ttgttcactt gactttaaga 60 aacccataaa gctgcctggc tttcagcaac aggcctatca acaccatggt gagtctccat 120 aagggacacc gtgt 134 38 644 DNA Homo sapiens 38 aagcctgttg tcatggggga ggtggtggcg cttggtggcc actggcggcc gaggtagagg 60 cagtggcgct tgagttggtc gggggcagcg gcagatttga ggcttaagca acttcttccg 120 gggaagagtg ccagtgcagc cactgttaca attcaagatc ttgatctata tccatagatt 180 ggaatattgg tgggccagca atcctcagac gcctcactta ggacaaatga ggaaactgag 240 gcttggtgaa gttacgaaac ttgtccaaaa tcacacaact tgtaaagggc acagccaaga 300 ttcagagcca ggctgtaaaa attaaaatga acaaattacg gcaaagtttt aggagaaaga 360 aggatgttta tgttccagag gccagtcgtc cacatcagtg gcagacagat gaagaaggcg 420 ttcgcaccgg aaaatgtagc ttcccggtta agtaccttgg ccatgtagaa gttgatgaat 480 caagaggaat gcacatctgt gaagatgctg taaaaagatt gaaagctgaa aggaagttct 540 tcaaaggctt ctttggaaaa actggaaaga aagcagttaa agcagtttct gtgggtctaa 600 gcagatggac tcagaggttg tggatgaaaa actaaggacc tcat 644 39 657 DNA Homo sapiens 39 ctttttgttt gggttttcca atgtagatgt ctcagtgaaa tgtgcagata tactttgttc 60 cttatatggt caccagtgtt aattatggac aaatacatta aaacaagggt tcctggccca 120 gcctcccatc taatctcttt gatactcttg gaatctaagt ctgaggagcg atttctgaat 180 tagccagtgt tgtaccaact ttctgttagg aattgtatta gaataacctt tctttttcag 240 acctgctcag tgagacatct tggggaatga agtaggaaaa tagacatttg gtggaaaaac 300 agcaaaatga gaacattaaa aagactcatt caagtatgag tataaagggc atggaaattc 360 tggtcctttg agcaaaatga gaagaaaaaa ttctgctcag cagtattcac tgtgttaaga 420 ttttttgttt tttacacgaa tggaaaaatg atgtgtaagt ggtatagatt ttaatcagct 480 aacagtcact ccagagattt tgatcagcac caattcctat agtagtaagt atttaaaagt 540 taagaaatac tactacattt aacattataa agtagagttc tggacataac tgaaaattag 600 atgtttgctt caatagaaat ttgttcccac ttgtattttc aacaaaatta tcggaac 657 40 1328 DNA Homo sapiens 40 acaattttaa aataactagc aattaatcac agcatatcag gaaaaagtac acagtgagtt 60 ctggttagtt tttgtaggct cattatggtt agggtcgtta agatgtatat aagaacctac 120 ctatcatgct gtatgtatca ctcattccat tttcatgttc catgcatact cgggcatcat 180 gctaatatgt atccttttaa gcactctcaa ggaaacaaaa gggcctttta tttttataaa 240 ggtaaaaaaa attccccaaa tattttgcac tgaatgtacc aaaggtgaag ggacattaca 300 atatgactaa cagcaactcc atcacttgag aagtataata gaaaatagct tctaaatcaa 360 acttccttca cagtgccgtg tctaccacta caaggactgt gcatctaagt aataattttt 420 taagattcac tatatgtgat agtatgatat gcatttattt aaaatgcatt agactctctt 480 ccatccatca aatactttac aggatggcat ttaatacaga tatttcgtat ttcccccact 540 gctttttatt tgtacagcat cattaaacac taagctcagt taaggagcca tcagcaacac 600 tgaagagatc agtagtaaga attccatttt ccctcatcag tgaagacacc acaaattgaa 660 actcagaact atatttctaa gcctgcattt tcactgatgc ataattttct tagtaatatt 720 aagagacagt ttttctatgg catctccaaa actgcatgac atcactagtc ttacttctgc 780 ttaattttat gagaaggtat tcttcatttt aattgctttt gggattactc cacatctttg 840 tttatttctt gactaatcag attttcaata gagtgaagtt aaattggggg tcataaaagc 900 attggattga catatggttt gccagcctat gggtttacag gcattgccca aacatttctt 960 tgagatctat atttataagc agccatggaa ttcctattat gggatgttgg caatcttaca 1020 ttttatagag gtcatatgca tagttttcat aggtgttttg taagaactga ttgctctcct 1080 gtgagttaag ctatgtttac tactgggacc ctcaagagga ataccactta tgttacactc 1140 ctgcactaaa ggcacgtact gcagtgtgaa gaaatgttct gaaaaagggt tatagaaatc 1200 tggaaataag aaaggaagag ctctctgtat tctataattg gaagagaaaa aaagaaaaac 1260 ttttaactgg aaatgttagt ttgtacttat tgatcatgaa tacaagtata tatttaattt 1320 tgaaaaaa 1328 41 987 DNA Homo sapiens 41 aacagagact ggcacaggac ctcttcattg caggaagatg gtagtgtagg caggtaacat 60 tgagctcttt tcaaaaaagg agagctcttc ttcaagataa ggaagtggta gttatggtgg 120 taacccccgg ctatcagtcc ggatggttgc cacccctcct gctgtaggat ggaagcagcc 180 atggagtggg agggaggcgc aataagacac ccctccacag agcttggcat catgggaagc 240 tggttctacc tcttcctggc tcctttgttt aaaggcctgg ctgggagcct tccttttggg 300 tgtctttctc ttctccaacc aacagaaaag actgctcttc aaaggtggag ggtcttcatg 360 aaacacagct gccaggagcc caggcacagg gctgggggcc tggaaaaagg agggcacaca 420 ggaggaggga ggagctggta gggagatgct ggctttacct aaggtctcga aacaaggagg 480 gcagaatagg cagaggcctc tccgtcccag gcccattttt gacagatggc gggacggaaa 540 tgcaatagac cagcctgcaa gaaagacatg tgttttgatg acaggcagtg tggccgggtg 600 gaacaagcac aggccttgga atccaatgga ctgaatcaga accctaggcc tgccatctgt 660 cagccgggtg acctgggtca attttagcct ctaaaagcct cagtctcctt atctgcaaaa 720 tgaggcttgt gatacctgtt ttgaagggtt gctgagaaaa ttaaagataa gggtatccaa 780 aatagtctac ggccatacca ccctgaacgt gcctaatctc gtaagctaag cagggtcagg 840 cctggttagt acctggatgg ggagagtatg gaaaacatac ctgcccgcag ttggagttgg 900 actctgtctt aacagtagcg tggcacacag aaggcactca gtaaatactt gttgaataaa 960 tgaagtagcg atttggtgtg aaaaaaa 987 42 956 DNA Homo sapiens 42 cggacggtgg ggcggacgcg tgggtgcagg agcagggcgg ctgccgactg ccccaaccaa 60 ggaaggagcc cctgagtccg cctgcgcctc catccatctg tccggccaga gccggcatcc 120 ttgcctgtct aaagccttaa ctaagactcc cgccccgggc tggccctgtg cagaccttac 180 tcaggggatg tttacctggt gctcgggaag ggaggggaag gggccgggga gggggcacgg 240 caggcgtgtg gcagccacac gcaggcggcc agggcggcca gggacccaaa gcaggatgac 300 cacgcacctc cacgccactg cctcccccga atgcatttgg aaccaaagtc taaactgagc 360 tcgcagcccc cgcgccctcc ctccgcctcc catcccgctt agcgctctgg acagatggac 420 gcaggccctg tccagccccc agtgcgctcg ttccggtccc cacagactgc cccagccaac 480 gagattgctg gaaaccaagt caggccaggt gggcggacaa aagggccagg tgcggcctgg 540 ggggaacgga tgctccgagg actggactgt ttttttcaca catcgttgcc gcagcggtgg 600 gaaggaaagg cagatgtaaa tgatgtgttg gtttacaggg tatatttttg ataccttcaa 660 tgaattaatt cagatgtttt acgcaaggaa ggacttaccc agtattactg ctgctgtgct 720 tttgatctct gcttaccgtt caagaggcgt gtgcaggccg acagtcggtg accccatcac 780 tcgcaggacc aagggggcgg ggactgctgg ctcacgcccc gctgtgtcct ccctcccctc 840 ccttccttgg gcagaatgaa ttcgatgcgt attctgtggc cgccatctgc gcagggtggt 900 ggtattctgt catttacaca cgtcgttcta attaaaaagc gaattatact ccaaaa 956 43 536 DNA Homo sapiens 43 aaataaacac ttccataaca ttttgttttc gaagtctatt aatgcaatcc cacttttttc 60 cccctagttt ctaaatgtta aagagagggg aaaaaaggct caggatagtt ttcacctcac 120 agtgttagct gtcttttatt ttactcttgg aaatagagac tccattaggg ttttgacatt 180 ttgggaaccc agttttacca ttgtgtcagt aaaacaataa gatagtttga gagcatatga 240 tctaaataaa gacatttgaa gggttagttt gaattctaaa agtaggtaat agccaaatag 300 cattctcatc ccttaacaga caaaaactta tttgtcaaaa gaattagaaa aggtgaaaat 360 attttttcca gatgaaactt gtgccacttc caattgacta atgaaataca aggagacaga 420 ctggaaaaag tgggttatgc cacctttaaa accctttctg gtaaatatta tggtagctaa 480 agggtggttt ccccggcacc tggacctgga caggtagggt tccgtggtta accagt 536 44 1630 DNA Homo sapiens 44 ggggagggac gagtatggaa ccctgaaggt agcaagtcca ggcactggcc tgaccatccg 60 gctccctggg caccaagtcc caggcaggag cagctgtttt ccatcccttc ccagacaagc 120 tctattttta tcacaatgac ctttagagag gtctcccagg ccagctcaag gtgtcccact 180 atcccctctg gagggaagag gcaggaaaat tctccccggg tccctgtcat gctactttct 240 ccatcccagt tcagactgtc caggacatct tatctgcagc cataagagaa ttataaggca 300 gtgatttccc ttaggcccag gacttgggcc tccagctcat ctgttccttc tgggcccatt 360 catggcaggt tctgggctca aagctgaact ggggagagaa gagatacaga gctaccatgt 420 gactttacct gattgccctc agtttggggt tgcttattgg gaaagagaga gacaaagagt 480 tacttgttac gggaaatatg aaaagcatgg ccaggatgca tagaggagat tctagcaggg 540 gacaggattg gctcagatga cccctgaggg ctcttccagt cttgaaatgc attccatgat 600 attaggaagt cgggggtggg tggtggtggt gggctagttg ggtttgaatt taggggccga 660 tgagcttggg tacgtgagca gggtgttaag ttagggtctg cctgtatttc tggtcccctt 720 ggaaatgtcc ccttcttcag tgtcagacct cagtcccagt gtccatatcg tgcccagaaa 780 agtagacatt atcctgcccc atcccttccc cagtgcactc tgacctagct agtgcctggt 840 gcccagtgac ctgggggagc ctggctgcag gccctcactg gttccctaaa ccttggtggc 900 tgtgattcag gtccccaggg gggactcagg gaggaatatg gctgagttct gtagtttcca 960 gagttggctg gtagagcctt ctagaggttc agaatattag cttcaggatc agctgggggt 1020 atggaattgg ctgaggatca aacgtatgta ggtgaaagga taccaggatg ttgctaaagg 1080 tgagggacag tttgggtttg ggacttacca gggtgatgtt agatctggaa cccccaagtg 1140 aggctggagg gagttaaggt cagtatggaa gatagggttg ggacagggtg ctttggaatg 1200 aaagagtgac cttagagggc tccttgggcc tcaggaatgc tcctgctgct gtgaagatga 1260 gaaggtgctc ttactcagtt aatgatgagt gactatattt accaaagccc ctacctgctg 1320 ctgggtccct tgtagcacag gagactgggg ctaagggccc ctcccaggga agggacacca 1380 tcaggcctct ggctgaggca gtagcataga ggatccattt ctacctgcat ttcccagagg 1440 actagcagga ggcagccttg agaaaccggc agttcccaag ccagcgcctg gctgttctct 1500 cattgtcact gccctctccc caacctctcc tctaacccac tagagattgc ctgtgtcctg 1560 cctcttgcct cttgtagaat gcagctctgg ccctcaataa atgcttcctg cattcatctg 1620 caaaaaaaaa 1630 45 169 DNA Homo sapiens 45 tcttttgctt ttagcttttt atttttgtat taacaggagt cttattacac ataggtctga 60 taaaactggt ttatgatctt cagtctgatt ccagtgctgc ataactagat aacgtatgaa 120 ggaaaaacga cgacgaacaa aaaagtaagt gcttggaaga cttagttga 169 46 769 DNA Homo sapiens 46 tgcaggtcat atttactatc ggcaataaaa ggaagcaaag cagtattaag cagcggtgga 60 atttgtcgct ttcacttttt ataaagtgct acataaaatg tcatatttcc aaatttaaaa 120 acataactcc agttcttacc atgagaacag catggtgatc acgaaggatc ttcttgaaaa 180 aaacaaaaac aaaaacaaaa aacaatgatc tcttctgggt atcacatcaa atgagataca 240 aaggtgtact aggcaatctt agagatctgg caacttattt tatatataag gcatctgtga 300 ccaagagacg ttatgaatta aatgtacaaa tgtattatgt ataaatgtat taaatgcaag 360 cttcatataa tgacaccaat gtctctaagt tgctcagaga tcttgactgg ctgtggccct 420 ggccagctcc tttcctgata gtctgattct gccttcatat ataggcagct cctgatcatc 480 catgccagtg aatgagaaaa caagcatgga atatataaac tttaacatta aaaaatgttt 540 tattttgtaa taaaatcaaa tttcccattg aaaccttcaa aaactttgca gaatgaggtt 600 ttgatatatg tgtacaagta gtaccttctt agtgcaagaa aacatcatta tttctgtctg 660 cctgcctttt tgtttttaaa aatgaagact atcattgaaa caagtttgtc ttcagtatca 720 ggacatgttg acggagagga aaggtaggaa agggttaggg atagaagcc 769 47 2529 DNA Homo sapiens 47 tttagttcat agtaatgtaa aaccatttgt ttaattctaa atcaaatcac tttcacaaca 60 gtgaaaatta gtgactggtt aaggtgtgcc actgtacata tcatcatttt ctgactgggg 120 tcaggacctg gtcctagtcc acaagggtgg caggaggagg gtggaggcta agaacacaga 180 aaacacacaa aagaaaggaa agctgccttg gcagaaggat gaggtggtga gcttgccgag 240 ggatggtggg aagggggctc cctgttgggg ccgagccagg agtcccaagt cagctctcct 300 gccttactta gctcctggca gagggtgagt ggggacctac gaggttcaaa atcaaatggc 360 atttggccag cctggcttta ctaacaggtt cccagagtgc ctctgttggc tgagctctcc 420 tgggctcact ccatttcatt gaagagtcca aatgattcat tttcctaccc acaacttttc 480 attattcttc tggaaaccca tttctgttga gtccatctga cttaagtcct ctctccctcc 540 actagttggg gccactgcac tgaggggggt cccaccaatt ctctctagag aagagacact 600 ccagaggccc ctgcaacttt gcggatttcc agaaggtgat aaaaagagca ctcttgagtg 660 ggtgcccagg aatgtttaaa atctatcagg cacactataa agctggtggt ttcttcctac 720 caagtggatt cggcatatga accacctact caatacttta tattttgtct gtttaaacac 780 tgaactctgg tgttgacagg tacaaaggag aagagatggg gactgtgaag aggggagggc 840 ttccctcatc ttcctcaaga tctttgtttc cataaactat gcagtcataa ttgagaaaaa 900 gcaatagatg gggcttccta ccatttgttg gttattgctg gggttagcca ggagcagtgt 960 ggatggcaaa gtaggagaga ggcccagagg aaagcccatc tccctccagc tttggggtct 1020 ccagaaagag gctggatttc tgggatgaag cctagaaggc agagcaagaa ctgttccacc 1080 aggtgaacag tcctacctgc ttggtaccat agtccctcaa taagattcag aggaagaagc 1140 ttatgaaact gaaaatcaaa tcaaggtatt gggaagaata atttcccctc gattccacag 1200 gagggaagac cacacaatat cattgtgctg gggctcccca aggccctgcc acctggcttt 1260 acaaatcatc aggggttgcc tgcttggcag tcacatgctt ccctggtttt agcacacata 1320 caaggagttt tcagggaact ctatcaagcc ataccaaaat cagggtcaca tgtgggtttc 1380 ccctttcctt gcctcttcat aaaagacaac ttggcttctg aggatggtgg tcttttgcat 1440 gcagttgggc tgacctgaca aagcccccag tttcctgtgg caggttctgg gagaggatgc 1500 attcaagctt ctgcagccta ggggacaggg ctgcttgttc agttattact gcctcggagc 1560 tccaaatccc accaaagtcc tgactccagg tctttcctaa tgcacagtag tcagtctcag 1620 cttcggcagt attctcggct gtatgttctc tggcagagag aggcagatga acatagtttt 1680 agggagaaag ctgatgggaa acctgtgagt taagccacat gtctcaccag gaataattta 1740 tgccaggaaa ccaggaagtc attcaagttg ttctctgagg ccaaagacac tgagcacagc 1800 ccagagccaa taaaagatct ttgagtctct ggtgaattca cgaagtgacc ccagctttag 1860 ctactgcaat tatgattttt atgggacagc aatttcttgc atctctacag aggaagaaga 1920 gggggagtgg gaggggaagg aaagagaaca gagcggcact gggatttgaa aggggaacct 1980 ctctatctga ggagccccca ctggcttcag aagcaactta ccaaggggta tttaaagaca 2040 tgaaaatttc cagaaatacc atttggtgca tccctttgtt tctgtaatat taaactcagg 2100 tgaaattata ctctgacagt ttctctcttt ctgcctcttc cctctgcaga gtcaggacct 2160 gcagaactgg ctgaaacaag atttcatggt gtcacccatg agagatgact caatgccaag 2220 gcctgaagtt atagagtgtt tacagcggtg gcgatattca ggggtcatcg ccaactggtc 2280 tcgagttcca aagctctgat gaagaaacaa gactccttga tgtgttactg atcccactga 2340 ttccaggagt caagattagc caggaagcca aacaccagga gttggggtgg cacgtcacca 2400 gtccagagcc ctgccacgga tgtacgcagg agcccagcat taggcaatca ggagccagaa 2460 catgatcacc agggccacaa ataggaagag gcgtgacagg aactgctcgt ccacatacct 2520 ggggtgtcc 2529 48 1552 DNA Homo sapiens 48 tttttttttt tttttgattt ctgggacaat taagctttat ttttcatata tatatatatt 60 ttcatatata tatatacata catatataaa ggaaacaatt tgcaaattta cacacctgac 120 aaaaccatat atacacacat atgtatgcat acacacagac agacacacac acccgaagct 180 ctagccaggc ccgttttcca tccctaagta ccattctctc atttgggccc ttctagggtt 240 ggggccctga gcttggtttg tagaagtttg gtgctaatat aaccatagct ttaatcccca 300 tgaaggacag tgtagacctc atctttgtct gctccccgct gcctttcagt tttacgtgat 360 ccatcaagag ggctatggga gccaagtgaa cacgggggat tgaggctaat tcacctgaac 420 tcgaaaacag cgcccagctt cctcaccgca ggcacgcgtc ttttcttttt ttttcctcga 480 gacggagtct cgctgtgttg cccaggctgg agtgcagtgg cacggtctcg gctcactgca 540 agctccacct cctggattca taccattctc ctgcttcagc cttccgagta gctgggacta 600 taggtgccaa ccactacgcc tagctaattt ttttttgtat ttttagtaga gacagggttt 660 caccgtgtta gccaggatgg tctcgtcctg actttgtgat ccgcccgcct cggcctccca 720 aagtgctggg attacaggcg tgagccacca cacctggccc cggcacgtat cttttaagga 780 atgacaccag ttcctggctt ctgaccaaag aaaaaatgtc acaggagact ttgaagaggc 840 agacaggagg gtggtggcag caacactgca gctgcttctg gatgctgctg gggtgctctc 900 cggagcgggt gtgaacagcg cacttcaaca tgagcaggcg cctggctccg gtgtgtcctc 960 acttcagtgg tgcacctgga tggtggaagc cagcctttgg ggcaggaaac cagctcagag 1020 aggctaccca gctcagctgc tggcaggagc caggtattta cagccataat gtgtgtaaag 1080 aaaaaacacg ttctgcaaga aactctccta cccgctcggg agactggggc tccttgcttg 1140 ggatgagctt cactcaacgt ggagatggtg gtggactggt ccctgaaaag cgggccttgc 1200 agggccaagt gaggtcctca ggtcctaacc cagtggccct ctgaaagggg gtgtgcaggc 1260 gaggggagca ggaggcttct ctctagtccc tttggaggct ttggctgaga gaagagtgag 1320 cagggagctg ggaatggtcc aggcagggaa gggagctgaa gtgattcggg gctaatgcct 1380 cagatcgatg tatttctctc cctggtctcc cggagccctc ttgtcaccgc tgctgccctg 1440 caggaggccc atctcttctg ggagcttatc tgacttaact tcaactacaa gttcgctctt 1500 acgagaccgg gggtagcgtg atctcctgct tccctgagcg cctgcacggc ag 1552 49 921 DNA Homo sapiens 49 ctgtggtccc agctactcag gaggctgagg cgggaggatt gcttgagccc aggagttgga 60 tgttgcagtg agccaagatc gcaccattgc cctccactct gggccacgga gcaataccct 120 gtctcagaaa acaaacaaca aaaagcagaa acgctgaagg ggtcggttta cgggaaaacc 180 gcctgtcaga acacttggct actcctaccc cagatcagtg gacctgggaa tgagggttgg 240 tcccgggagg cttttctcca agctgttgcc accagacccg ccatgggaac cctggccaca 300 gaagcctccc ggggagtgag ccagagcctg gaccgctgtg ctgatgtgtc tggggtggag 360 ggagggtggg gagtgtgcaa gggtgtgtgt gtgcccgggg ggtgttcatg ggcaagcatg 420 tgcgtgcctg tgtgtgtgcg tgcccctccc ctgcagccgt cggtggtatc tccctccagc 480 cccttcgcca ccttctgagc attgtctgtc cacgtgagac tgcccagaga cagcagagct 540 ccacgtggtt ttaaggggag acctttccct ggacctgggg gtctcgccgt atctcatgac 600 caggtgctaa atgacccgac atgcatcacc tgcctttcga tgaccaacct ccctgtcccc 660 gtcccgctga cctgcccccg tggcgtctca cggtgatgcc tgctcctgac attggtgttc 720 actgtagcaa actacattct ggatgggaat tttcatgtac atgtgtggca tgtggaaaat 780 ttcaaataaa atggacttga tttagaaagc caaaaagctg tgtggtcctt ccagcacgga 840 tactttgacc tcttgcctac aaccccttcc ttgggtccga ggctggtagc tttgttcact 900 tcagatggtt gggggcgggt g 921 50 338 DNA Homo sapiens 50 atgatctatc tagatgccct accgtaaaat caaaacacaa aaccctactg actcattccc 60 tcccttccag atattacccc atttctctac ttcccattgt agccaaactt tccaaaaatt 120 catgttctgt cttcatttcc tcatgttcaa cccaccctgt cttagctacc acccctcagt 180 aacgacctag cctgggtaga aacaaatgtc agcatgatac catactcaat gatccttcgt 240 cactgttgtc attgtcatca ttccatggcc ttactttccc tctcagcgcc atttgctaca 300 gtaagaaact ttctttcttg aattcttggt tctcttgg 338 51 1191 DNA Homo sapiens 51 ctagcaagca ggtaaacgag ctttgtacaa acacacacag accaacacat ccggggatgg 60 ctgtgtgttg ctagagcaga ggctgattaa acactcagtg tgttggctct ctgtgccact 120 cctggaaaat aatgaattgg gtaaggaaca gttaataaga aaatgtgcct tgctaactgt 180 gcacattaca acaaagagct ggcagctcct gaaggaaaag ggcttgtgcc gctgccgttc 240 aaacttgtca gtcaactcat gccagcagcc tcagcgtctg cctccccagc acaccctcat 300 tacatgtgtc tgtctggcct gatctgtgca tctgctcgga gacgctcctg acaagtcggg 360 aatttctcta tttctccact ggtgcaaaga gcggatttct ccctgcttct cttctgtcac 420 ccccgctcct ctcccccagg aggctccttg atttatggta gctttggact tgcttccccg 480 tctgactgtc cttgacttct agaatggaag aagctgagct ggtgaaggga agactccagg 540 ccatcacaga taaaagaaaa atacaggaag aaatctcaca gaagcgtctg aaaatagagg 600 aagacaaact aaagcaccag catttgaaga aaaaggcctt gagggagaaa tggcttctag 660 atggaatcag cagcggaaaa gaacaggaag agatgaagaa gcaaaatcaa caagaccagc 720 accagatcca ggttctagaa caaagtatcc tcaggcttga gaaagagatc caagatcttg 780 aaaaagctga actgcaaatc tcaacgaagg aagaggccat tttaaagaaa ctaaagtcaa 840 ttgagcggac aacagaagac attataagat ctgtgaaagt ggaaagagaa gaaagagcag 900 aagagtcaat tgaggacatc tatgctaata tccctgacct tccaaagtcc tacatacctt 960 ctaggttaag gaaggagata aatgaagaaa aagaagatga tgaacaaaat aggaaagctt 1020 tatatgccat ggaaattaaa gttgaaaaag acttgaagac tggagaaagt acagttctgt 1080 cttccaatac ctctggccat cagatgactt taaaaggtac aggagtaaaa gtttaagatg 1140 atgggcaaaa gtccagtgta ttcagtaaag tgctaatcac aagttggagg t 1191 52 1200 DNA Homo sapiens 52 aacagggact ctcactctat caaccccagg ctggagtccg gtgcgcccac cctggctccc 60 tgcaacctcc gcctcccagg ctcaagcaac tctcctgcct cagtcgctct agtagctggg 120 actacaggca cacaccacca tgcccagcca atttttgcat tttttgtaga gacagggttt 180 cgccttctgt ccaggccggc atcatatact ttaaatcatg cccagatgac tttaatacct 240 aatacaatat atcaggttgg tttaaaaata attgcttttt tattattttt gcatttttgc 300 accaacctta atgctatgta aatagttgtt atactgttgc ttaacaacag tatgacaatt 360 ttggcttttt ctttgtatta ttttgtattt ttttttttta ttgtgtggtc tttttttttt 420 ttctcagtgt tttcaattcc tccttggttg aatccatgga tgcaaaaccc acagatatga 480 agggctggct atatatgcat tgatgattgt cctattatat tagttataaa gtgtcattta 540 atatgtagtg aaagttatgg tacagtggaa agagtagttg aaaacataaa catttggacc 600 tttcaagaaa ggtagcttgg tgaagttttt caccttcaaa ctatgtccca gtcagggctc 660 tgctactaat tagctataat ctttgcacaa attacatcac ctttgagtct cagttgcctc 720 acctgtaaaa tgaaagaact ggatactctc taaggtcact tccagccctg tcattctata 780 actctgttat gctgaggaag aaattcacat tgtgttaact gtatgagtca aactgaaaat 840 gattattaaa gtgggaaaaa gccaattgct tctcttagaa agctcaacta aatttgagaa 900 gaataatctt ttcaattttt taagaattta aatattttta agggtttgac ctatttattt 960 agagatgggg tctcactctg tcacccagac tggagtacag tggcacaatc atagctcact 1020 gctgcctcaa attcatgggc tcaagtgatc ctcctgcctc tgcctccaga gtagctgcga 1080 ctatgggcat gtgccaccac gcctggctaa catttgtatt gacctattta tttattgtga 1140 tttatatctt tttttttttt tctttttttt ttttttacaa aatcagaaat acttattttg 1200 53 989 DNA Homo sapiens 53 aagccaccac tcaaaacttc ctatacattt tcacagcaga gacaagtgaa catttatttt 60 tatgcctttc ttcctatgtg tatttcaagt ctttttcaaa acaaggcccc aggactctcc 120 gattcaatta gtccttgggc tggtcgactg tgcaggagtc cagggagcct ctacaaatgc 180 agagtgactc tttaccaaca taaaccctag atacatgcaa aaagcaggac ccttcctcca 240 ggaatgtgcc atttcagatg cacagcaccc atgcagaaaa gctggaattt tccttggaac 300 cgactgtgat agaggtgctt acatgaacat tgctactgtc tttctttttt tttgagacag 360 gtttcgcttg tgcccaggct gagtgcaatg cgtgatctca ctcactgcaa ttccacctcc 420 aggttcaagc attctcctgc tcagcctcct agtagctggg ttacaggcac tgccaccatg 480 ccggctaatt ttgtattttt gtagagatgg atttctccat ttggtcaggc ggtctcgaac 540 cccaacctca gtgatctgcc acctcagcct cctaagtgtt ggattacagg atgagccacc 600 cgaccggcca ctactgtctt tctttgaccc ttccagtttc gaagataaag aggaaataat 660 ttctctgaag tacttgataa aatttccaaa caaaacacat gtccacttca ctgataaaaa 720 atttaccgca gtttggcacc taagagtatg acaacagcaa taaaaagtaa tttcaaagag 780 ttaagatttc ttcagcaaaa tagatgattc acatcttcaa gtcctttttg aaatcagtta 840 ttaatattat tctttcctca tttccatctg aatgactgca gcaatagttt tttttttttt 900 tttttttttt ttgcgagatg gaatctcgct ctgtcgccca gcgggagtgc actggcgcaa 960 gcccggctca ccgcaatctc tgccacccg 989 54 250 DNA Homo sapiens 54 catttcccca ttggtcctga tgttgaagat ttagttaaag aggctgtaag tcaggttcga 60 gcagaggcta ctacaagaag tagggaatca agtccctcac atgggctatt aaaactaggt 120 agtggtggag tagtgaaaaa gaaatctgag caacttcata acgtaactgc ctttcaggga 180 aaagggcatt ctttaggaac tgcatctggt aacccacacc ttgatccaag agctagggaa 240 acttcagttg 250 55 2270 DNA Homo sapiens 55 gcgcccccga gcagcgcccg cgccctccgc gccttctccg ccgggacctc gagcgaaaga 60 ggcccgcgcg ccgcccagcc ctcgcctccc tgcccaccgg gcacaccgcg ccgccacccc 120 gaccccgctg cgcacggcct gtccgctgca caccagcttg ttggcgtctt cgtcgccgcg 180 ctcgccccgg gctactcctg cgcgccacaa tgagctcccg catcgccagg gcgctcgcct 240 tagtcgtcac ccttctccac ttgaccaggc tggcgctctc cacctgcccc gctgcctgcc 300 actgccccct ggaggcgccc aagtgcgcgc cgggagtcgg gctggtccgg gacggctgcg 360 gctgctgtaa ggtctgcgcc aagcagctca acgaggactg cagcaaaacg cagccctgcg 420 accacaccaa ggggctggaa tgcaacttcg gcgccaagtc caccgctctg aaggggatct 480 gcagagctca gtcagagggc agaccctgtg aatataactc cagaatctac caaaacgggg 540 aaagtttcca gcccaactgt aaacatcagt gcacatgtat tgatggcgcc gtgggctgca 600 ttcctctgtg tccccaagaa ctatctctcc ccaacttggg ctgtcccaac cctcggctgg 660 tcaaagttac cgggcagtgc tgcgaggagt gggtctgtga cgaggatagt atcaaggacc 720 ccatggagga ccaggacggc ctccttggca aggagctggg attcgatgcc tccgaggtgg 780 agttgacgag aaacaatgaa ttgattgcag ttggaaaagg cagctcactg aagcggctcc 840 ctgtttttgg aatggagcct cgcatcctat acaacccttt acaaggccag aaatgtattg 900 ttcaaacaac ttcatggtcc cagtgctcaa agacctgtgg aactggtatc tccacacgag 960 ttaccaatga caaccctgag tgccgccttg tgaaagaaac ccggatttgt gaggtgcggc 1020 cttgtggaca gccagtgtac agcagcctga aaaagggcaa gaaatgcagc aagaccaaga 1080 aatcccccga accagtcagg tttacttacg ctggatgttt gagtgtgaag aaataccggc 1140 ccaagtactg cggttcctgc gtggacggcc gatgctgcac gccccagctg accaggactg 1200 tgaagatgcg gttccgctgc gaagatgggg agacattttc caagaacgtc atgatgatcc 1260 agtcctgcaa atgcaactac aactgcccgc atgccaatga agcagcgttt cccttctaca 1320 ggctgttcaa tgacattcac aaatttaggg actaaatgct acctgggttt ccagggcaca 1380 cctagacaaa caagggagaa gagtgtcaga atcagaatca tggagaaaat gggcgggggt 1440 ggtgtgggtg atgggactca ttgtagaaag gaagccttgc tcattcttga ggagcattaa 1500 ggtatttcga aactgccaag ggtgctggtg cggatggaca ctaatgcagc cacgattgga 1560 gaatactttg cttcatagta ttggagcaca tgttactgct tcattttgga gcttgtggag 1620 ttgatgactt tctgttttct gtttgtaaat tatttgctaa gcatattttc tctaggcttt 1680 tttccttttg gggttctaca gtcgtaaaag agataataag attagttgga cagtttaaag 1740 cttttattcg tcctttgaca aaagtaaatg ggagggcatt ccatcccttc ctgaaggggg 1800 acactccatg agtgtctgtg agaggcagct atctgcactc taaactgcaa acagaaatca 1860 ggtgttttaa gactgaatgt tttatttatc aaaatgtagc ttttggggag ggaggggaaa 1920 tgtaatactg gaataatttg taaatgattt taattttata ttcagtgaaa agattttatt 1980 tatggaatta accatttaat aaagaaatat ttacctaata tctgagtgta tgccattcgg 2040 tatttttaga ggtgctccaa agtcattagg aacaacctag ctcacgtact caattattca 2100 aacaggactt attgggatac agcagtgaat taagctatta aaataagata atgattgctt 2160 ttataccttc agtagagaaa agtctttgca tataaagtaa tgtttaaaaa acatgtattg 2220 aacacgacat tgtatgaagc acaataaaga ttctgaagct aaaaaaaaaa 2270 56 1636 DNA Homo sapiens 56 cttgaatgaa gctgacacca agaaccgcgg gaagagcttg ggcccaaagc aggaaaggga 60 agcgctcgag ttggaaagga accgctgctg ctggccgaac tcaagcccgg gcgcccccac 120 cagtttgatt ggaagtccag ctgtgaaacc tggagcgtcg ccttctcccc agatggctcc 180 tggtttgctt ggtctcaagg acactgcatc gtcaaactga tcccctggcc gttggaggag 240 cagttcatcc ctaaagggtt tgaagccaaa agccgaagta gcaaaaatga gacgaaaggg 300 cggggcagcc caaaagagaa gacgctggac tgtggtcaga ttgtctgggg gctggccttc 360 agcccgtggc cttccccacc cagcaggaag ctctgggcac gccaccaccc ccaagtgccc 420 gatgtctctt gcctggttct tgctacggga ctcaacgatg ggcagatcaa gatctgggag 480 gtgcagacag ggctcctgct tttgaatctt tccggccacc aagatgtcgt gagagatctg 540 agcttcacac ccagtggcag tttgattttg gtctccgcgt cacgggataa gactcttcgc 600 atctgggacc tgaataaaca cggtaaacag attcaagtgt tatcgggcca cctgcagtgg 660 gtttactgct gttccatctc cccagactgc agcatgctgt gctctgcagc tggagagaag 720 tcggtctttc tatggagcat gaggtcctac acgttaattc ggaagctaga gggccatcaa 780 agcagtgttg tctcttgtga cttctccccc gactctgccc tgcttgtcac ggcttcttac 840 gataccaatg tgattatgtg ggacccctac accggcgaaa ggctgaggtc actccaccac 900 acccaggttg accccgccat ggatgacagt gacgtccaca ttagctcact gagatctgtg 960 tgcttctctc cagaaggctt gtaccttgcc acggtggcag atgacagact cctcaggatc 1020 tgggccctgg aactgaaaac tcccattgca tttgctccta tgaccaatgg gctttgctgc 1080 acattttttc cacatggtgg agtcattgcc acagggacaa gagatggcca cgtccagttc 1140 tggacagctc ctagggtcct gtcctcactg aagcacttat gccggaaagc ccttcgaagt 1200 ttcctaacaa cttaccaagt cctagcactg ccaatcccca agaaaatgaa agagttcctc 1260 acatacagga ctttttaagc aacaccacat cttgtgcttc tttgtagcag ggtaaatcgt 1320 cctgtcaaag ggagttgctg gaataatggg ccaaacatct ggtcttgcat tgaaatagca 1380 tttctttggg attgtgaata gaatgtagca aaaccagatt ccagtgtaca taaaagaatt 1440 tttttgtctt taaatagata caaatgtcta tcaactttaa tcaagttgta acttatattg 1500 aagacaattt gatacataat aaaaaattat gacaatgtcc tgggaaaaaa aaaatgtaga 1560 aagatggtga agggtgggat ggatgaggag cgtggtgacg ggggcctgca gcgggttggg 1620 gaccctgtgc tgcgtt 1636 57 460 DNA Homo sapiens 57 ccatgtgtgt atgagagaga gagagattgg gagggagagg gagctcacta gcgcatatgt 60 gcctccaggg ggctgcagat gtgtctgagg gtgagcctgg tgaaagagaa gacaaaagaa 120 tggaatgagc taaagcagcc gcctggggtg ggaggccgag cccatttgta tgcagcaggg 180 ggcaggagcc cagcaaggga gcctccattc ccaggactct ggagggagct gagaccatcc 240 atgcccgcag agccctccct cacactccat cctgtccagc cctaattgtg caggtgggga 300 aactgaggct gggaagtcac atagcaagtg actggcagag ctgggactgg aacccaacca 360 gcctcctaga ccacggttct tcccatcaat ggaatgctag agactccagc caggtgggta 420 ccgagctcga attcgtaatc atggtcatag ctgtttcctg 460 58 1049 DNA Homo sapiens 58 atctgatcaa gaatacctgc cctggtcact ctgcggatgt ttctgtccac ttgttcacat 60 tgaggaccaa gatatccttt tttacagagg cacttgttcg gtctaacaca gacacctcca 120 tgacgacatg ctggctcaca ttttgcagtt ctgcagaagt ccccctccca gcctggacta 180 cagcagcact ttcccgtggg ggtgcagtag ccgtttcgac agagcctgga gcactctgaa 240 gtcagtgtct gtgcaggttg taccgtggct ctgcattcct caggcattaa aggtcttttg 300 ggatctacaa ttttgtagag ttttccattg tgagtctggg tcatactttt actgcttgat 360 aaaatgtaaa cttcacctag ttcatcttct ccaaatccca agatgtgacc ggaaaagtag 420 cctctacagg acccactagt gccgacacag agtggttttt cttgccactg ctttgtcaca 480 ggactttgct ggagagttag gaaattccca ttacgatctc caaacacgta gcttccatac 540 aatctttctg actggcagcc ccggtataca aatccaccaa ccaaaggacc attactgaat 600 ggcttgaatt ctaaaagtga tggctcactt tcataatctt tcccctttat tatctgtaga 660 attctggctg atgatctgtt ttttccattg gagtctgaac acagtatcgt taaattgatg 720 tttatatcag tgggatgtct atccacagca catctgcctg gatcgtggag cccatgagca 780 aacacttcgg ggggctggtt ggtgctgttg aagtgtgggt tgctccttgg tatggaataa 840 ggcacgttgc acatgtctgt gtccacatcc agccgtagca ctgagcctgt gaaatcactt 900 aacccatcca tttcttccat atcatccagt gtaatcatcc catcaccaag aatgatgtac 960 aaaaacccgt cagggccaaa gagcagttgc cctcccagat gctttctgtg gagttctgca 1020 acttcaagaa agactctggc tgttctcaa 1049 59 747 DNA Homo sapiens 59 tttttcaaat cacatatggc ttctttgacc ccatcaaata actttattca cacaaacgtc 60 ccttaattta caaagcctca gtcattcata cacattaggg gatccacagt gttcaaggaa 120 cttaaatata atgtatcata ccaacccaag taaaccaagt acaaaaaata ttcatataaa 180 gttgttcaca cgtaggtcct agattaccag cttctgtgca aaaaaaggaa atgaagaaaa 240 atagatttat taactagtat tggaaactaa ctttgtgcct ggcttaaaac ctccctcacg 300 ctcgtctgtc ccacacaaat gtttaagaag tcactgcaat gtactccccg gctctgatga 360 aaagaagccc ctggcacaaa agattccagt gcccctgaag aggctccctt cctcctgtgg 420 gctctcctag aaaaccagcg ggacggcctc cctgctgata ccgtctataa ccttaggggg 480 ccctcgggca ggcaacggca gtggactcat ctcggtgatg gctgtagatg ctaacactgg 540 ccaattcaat gccacaccta ctggttaccc tttgagggca tttctccaga cagaagcccc 600 ttgaagccta ggtagggcag gatcagagat acacccgtgt ttgtctcgaa gggctccaca 660 gcccagtacg acatgcttgc agaagtagta tctctggact tctgcctcca gtcgaccggc 720 cgcgaattta gtagtaatag cggccgc 747 60 1036 PRT Homo sapiens 60 Met Tyr Leu Val Ala Gly Asp Arg Gly Leu Ala Gly Cys Gly His Leu 1 5 10 15 Leu Val Ser Leu Leu Gly Leu Leu Leu Leu Pro Ala Arg Ser Gly Thr 20 25 30 Arg Ala Leu Val Cys Leu Pro Cys Asp Glu Ser Lys Cys Glu Glu Pro 35 40 45 Arg Asn Arg Pro Gly Ser Ile Val Gln Gly Val Cys Gly Cys Cys Tyr 50 55 60 Thr Cys Ala Ser Gln Gly Asn Glu Ser Cys Gly Gly Thr Phe Gly Ile 65 70 75 80 Tyr Gly Thr Cys Asp Arg Gly Leu Arg Cys Val Ile Arg Pro Pro Leu 85 90 95 Asn Gly Asp Ser Leu Thr Glu Tyr Glu Ala Gly Val Cys Glu Asp Glu 100 105 110 Asn Trp Thr Asp Asp Gln Leu Leu Gly Phe Lys Pro Cys Asn Glu Asn 115 120 125 Leu Ile Ala Gly Cys Asn Ile Ile Asn Gly Lys Cys Glu Cys Asn Thr 130 135 140 Ile Arg Thr Cys Ser Asn Pro Phe Glu Phe Pro Ser Gln Asp Met Cys 145 150 155 160 Leu Ser Ala Leu Lys Arg Ile Glu Glu Glu Lys Pro Asp Cys Ser Lys 165 170 175 Ala Arg Cys Glu Val Gln Phe Ser Pro Arg Cys Pro Glu Asp Ser Val 180 185 190 Leu Ile Glu Gly Tyr Ala Pro Pro Gly Glu Cys Cys Pro Leu Pro Ser 195 200 205 Arg Cys Val Cys Asn Pro Ala Gly Cys Leu Arg Lys Val Cys Gln Pro 210 215 220 Gly Asn Leu Asn Ile Leu Val Ser Lys Ala Ser Gly Lys Pro Gly Glu 225 230 235 240 Cys Cys Asp Leu Tyr Glu Cys Lys Pro Val Phe Gly Val Asp Cys Arg 245 250 255 Thr Val Glu Cys Pro Thr Val Gln Gln Thr Ala Cys Pro Pro Asp Ser 260 265 270 Tyr Glu Thr Gln Val Arg Leu Thr Ala Asp Gly Cys Cys Thr Leu Pro 275 280 285 Thr Arg Cys Glu Cys Leu Ser Gly Leu Cys Gly Phe Pro Val Cys Glu 290 295 300 Val Gly Ser Thr Pro Arg Ile Val Ser Arg Gly Asp Gly Thr Pro Gly 305 310 315 320 Lys Cys Cys Asp Val Phe Glu Cys Val Asn Asp Thr Lys Pro Ala Cys 325 330 335 Val Phe Asn Asn Val Glu Tyr Tyr Asp Gly Asp Met Phe Arg Met Asp 340 345 350 Asn Cys Arg Phe Cys Arg Cys Gln Gly Gly Val Ala Ile Cys Phe Thr 355 360 365 Ala Gln Cys Gly Glu Ile Asn Cys Glu Arg Tyr Tyr Val Pro Glu Gly 370 375 380 Glu Cys Cys Pro Val Cys Glu Asp Pro Val Tyr Pro Phe Asn Asn Pro 385 390 395 400 Ala Gly Cys Tyr Ala Asn Gly Leu Ile Leu Ala His Gly Asp Arg Trp 405 410 415 Arg Glu Asp Asp Cys Thr Phe Cys Gln Cys Val Asn Gly Glu Arg His 420 425 430 Cys Val Ala Thr Val Cys Gly Gln Thr Cys Thr Asn Pro Val Lys Val 435 440 445 Pro Gly Glu Cys Cys Pro Val Cys Glu Glu Pro Thr Ile Ile Thr Val 450 455 460 Asp Pro Pro Ala Cys Gly Glu Leu Ser Asn Cys Thr Leu Thr Arg Lys 465 470 475 480 Asp Cys Ile Asn Gly Phe Lys Arg Asp His Asn Gly Cys Arg Thr Cys 485 490 495 Gln Cys Ile Asn Thr Gln Glu Leu Cys Ser Glu Arg Lys Gln Gly Cys 500 505 510 Thr Leu Asn Cys Pro Phe Gly Phe Leu Thr Asp Ala Gln Asn Cys Glu 515 520 525 Ile Cys Glu Cys Arg Pro Arg Pro Lys Lys Cys Arg Pro Ile Ile Cys 530 535 540 Asp Lys Tyr Cys Pro Leu Gly Leu Leu Lys Asn Lys His Gly Cys Asp 545 550 555 560 Ile Cys Arg Cys Lys Lys Cys Pro Glu Leu Ser Cys Ser Lys Ile Cys 565 570 575 Pro Leu Gly Phe Gln Gln Asp Ser His Gly Cys Leu Ile Cys Lys Cys 580 585 590 Arg Glu Ala Ser Ala Ser Ala Gly Pro Pro Ile Leu Ser Gly Thr Cys 595 600 605 Leu Thr Val Asp Gly His His His Lys Asn Glu Glu Ser Trp His Asp 610 615 620 Gly Cys Arg Glu Cys Tyr Cys Leu Asn Gly Arg Glu Met Cys Ala Leu 625 630 635 640 Ile Thr Cys Pro Val Pro Ala Cys Gly Asn Pro Thr Ile His Pro Gly 645 650 655 Gln Cys Cys Pro Ser Cys Ala Asp Asp Phe Val Val Gln Lys Pro Glu 660 665 670 Leu Ser Thr Pro Ser Ile Cys His Ala Pro Gly Gly Glu Tyr Phe Val 675 680 685 Glu Gly Glu Thr Trp Asn Ile Asp Ser Cys Thr Gln Cys Thr Cys His 690 695 700 Ser Gly Arg Val Leu Cys Glu Thr Glu Val Cys Pro Pro Leu Leu Cys 705 710 715 720 Gln Asn Pro Ser Arg Thr Gln Asp Ser Cys Cys Pro Gln Cys Thr Asp 725 730 735 Gln Pro Phe Arg Pro Ser Leu Ser Arg Asn Asn Ser Val Pro Asn Tyr 740 745 750 Cys Lys Asn Asp Glu Gly Asp Ile Phe Leu Ala Ala Glu Ser Trp Lys 755 760 765 Pro Asp Val Cys Thr Ser Cys Ile Cys Ile Asp Ser Val Ile Ser Cys 770 775 780 Phe Ser Glu Ser Cys Pro Ser Val Ser Cys Glu Arg Pro Val Leu Arg 785 790 795 800 Lys Gly Gln Cys Cys Pro Tyr Cys Ile Lys Asp Thr Ile Pro Lys Lys 805 810 815 Val Val Cys His Phe Ser Gly Lys Ala Tyr Ala Asp Glu Glu Arg Trp 820 825 830 Asp Leu Asp Ser Cys Thr His Cys Tyr Cys Leu Gln Gly Gln Thr Leu 835 840 845 Cys Ser Thr Val Ser Cys Pro Pro Leu Pro Cys Val Glu Pro Ile Asn 850 855 860 Val Glu Gly Ser Cys Cys Pro Met Cys Pro Glu Met Tyr Val Pro Glu 865 870 875 880 Pro Thr Asn Ile Pro Ile Glu Lys Thr Asn His Arg Gly Glu Val Asp 885 890 895 Leu Glu Val Pro Leu Trp Pro Thr Pro Ser Glu Asn Asp Ile Val His 900 905 910 Leu Pro Arg Asp Met Gly His Leu Gln Val Asp Tyr Arg Asp Asn Arg 915 920 925 Leu His Pro Ser Glu Asp Ser Ser Leu Asp Ser Ile Ala Ser Val Val 930 935 940 Val Pro Ile Ile Ile Cys Leu Ser Ile Ile Ile Ala Phe Leu Phe Ile 945 950 955 960 Asn Gln Lys Lys Gln Trp Ile Pro Leu Leu Cys Trp Tyr Arg Thr Pro 965 970 975 Thr Lys Pro Ser Ser Leu Asn Asn Gln Leu Val Ser Val Asp Cys Lys 980 985 990 Lys Gly Thr Arg Val Gln Val Asp Ser Ser Gln Arg Met Leu Arg Ile 995 1000 1005 Ala Glu Pro Asp Ala Arg Phe Ser Gly Phe Tyr Ser Met Gln Lys Gln 1010 1015 1020 Asn His Leu Gln Ala Asp Asn Phe Tyr Gln Thr Val 1025 1030 1035 

1. Pharmaceutical compositions comprising one or several agents as compound I which modulate the biological function of one or several of the VEGF/VEGF receptor systems, and comprising one or several agents as compound II which modulate the biological function of one or several of the Angiopoietin/Tie receptor systems.
 2. Pharmaceutical compositions comprising one or several agents as compound I which are targeted to the endothelium via of one or several of the VEGF/VEGF receptor systems, and comprising one or several agents as compound II which modulate the biological function of one or several of the Angiopoietin/Tie receptor systems.
 3. Pharmaceutical compositions comprising one or several agents as compound I which modulates the biological function of one or several of the VEGF/VEGF receptor systems or of one or several of the Angiopoietin/Tie receptor systems and comprising one or several agents as compound II which are targeted to the endothelium.
 4. Pharmaceutical compositions comprising one or several agents as compound I which modulate the biological function of one or several of the VEGF/VEGF receptor systems, and comprising one or several agents as compound II which are targeted to the endothelium via one or several of the Angiopoietin/Tie receptor systems.
 5. Pharmaceutical compositions comprising one or several agents as compound I which are targeted to the endothelium via one or several of the VEGF/VEGF receptor systems, and comprising one or several agents as compound II which are targeted to the endothelium via one or several of the Angiopoietin/Tie receptor systems.
 6. Pharmaceutical compositions comprising one or several agents as compound I which modulate the biological function of one or several of the VEGF/VEGF receptor systems, and comprising one or several agents as compound II which are targeted to the endothelium via one or several of the VEGF/VEGF receptor systems.
 7. Pharmaceutical compositions comprising one or several agents as compound I which modulate the biological function of one or several of the Angiopoietin/Tie receptor systems, and comprising one or several agents as compound II which are targeted to the endothelium via one or several of the Angiopoietin/Tie receptor systems.
 8. Pharmaceutical compositions comprising one or several agents which interfere with both the function of one or several of the VEGF/VEGF receptor systems and the function of one or several of the Angiopoietin/Tie receptor systems.
 9. Pharmaceutical compositions according to claims 1-8 which are intended for simultaneous or separate sequential therapeutical application.
 10. Pharmaceutical compositions according to claims 1-8 which comprise as compound I at least one of a) compounds which inhibit receptor tyrosine kinase activity, b) compounds which inhibit ligand binding to receptors, c) compounds which inhibit activation of intracellular signal pathways of the receptors, d) compounds which inhibit or activate expression of a ligand or of a receptor of the VEGF or Tie receptor system, e) delivery systems, such as antibodies, ligands, high-affinity binding oligonucleotides or oligopeptides, or liposomes, which target cytotoxic agents or coagulation-inducing agents to the endothelium via recognition of VEGF/VEGF receptor or Angiopoietin/Tie receptor systems, f) delivery systems, such as antibodies, ligands, high-affinity binding oligonucleotides or oligopeptides, or liposomes, which are targeted to the endothelium and induce necrosis or apoptosis.
 11. Pharmaceutical compositions according to claims 1-8 which comprise as compound II at least one of g) compounds which inhibit receptor tyrosine kinase activity, h) compounds which inhibit ligand binding to receptors, i) compounds which inhibit activation of intracellular signal pathways of the receptors, j) compounds which inhibit or activate expression of a ligand or of a receptor of the VEGF or Tie receptor system, k) delivery systems, such as antibodies, ligands, high-affinity binding oligonucleotides or oligopeptides, or liposomes, which target cytotoxic agents or coagulation-inducing agents to the endothelium via recognition of VEGF/VEGF receptor or Angiopoietin/Tie receptor systems, l) delivery systems, such as antibodies, ligands, high-affinity binding oligonucleotides or oligopeptides, or liposomes, which are targeted to the endothelium and induce necrosis or apoptosis.
 12. Pharmaceutical compositions according to claims 1-11 which comprise as compound I and/or II at least one of Seq. ID Nos. 1-59.
 13. Pharmaceutical compositions according to claims 1-11 which comprise as compound I and/or II Seq. ID Nos. 34a
 14. Pharmaceutical compositions according to claims 1-11 which comprise as compound I and/or II at least one of sTie2, mAB 4301-42-35, scFv-tTF and/or L19 scFv-tTF conjugate.
 15. Pharmaceutical compositions according to claims 1-11 which comprise as compound I and/or II at least one small molecule of genaral formula I

in which r has the meaning of 0 to 2, n has the meaning of 0 to 2; R₃ und R₄ a) each independently from eaxh other have the meaning of lower alkyl, b) together form a bridge of general partial formula II,

wherein the binding is via the two terminal C-atoms, and m has the meaning of 0 to 4; or c) together form a bridge of partial formula III

wherein one or two of the ring members T₁,T₂,T₃,T₄ has the meaning of nitrogen, and each others have the meaning of CH, and the bining is via the atoms T₁ and T₄; G has the meaning of C₁-C₆-alkyl, C₂-C₆-alkylene or C₂-C₆-alkenylene; or C₂-C₆-alkylene or C₃-C₆-alkenylene, which are substituted with acyloxy or hydroxy; —CH₂—O—, —CH₂—S—, —CH₂—NH—, —CH₂—O—CH₂—, —CH₂—S—CH₂—, —CH₂—NH—CH₂, oxa (—O—), thia (—S—) or imino (—NH—), A, B, D, E and T independently from each other have the meaning of N or CH, with the provisio that not more than three of these Substituents have the meaning of N, Q has the meaning of lower alkyl, lower alkyloxy or halogene, R¹ and R₂ independently from each other have the meaning of H or lower alkyl, X has the meaning of imino, oxa or thia; Y has the meaning of hydrogene, unsubstituted or substituted aryl, heteroaryl, or unsubstituted or substituted cycloalkyl; and Z has the meaning of amino, mono- or disubstituted amino, halogen, alkyl, substituted alkyl, hydroxy, etherificated or esterificated hydroxy, nitro, cyano, carboxy, esterificated carboxy, alkanoyl, carbamoyl, N-mono- or N,N-disubstituted carbamoyl, amidino, guanidino, mercapto, sulfo, phenylthio, phenyl-lower-alkyl-thio, alkyl-phenyl-thio, phenylsulfinyl, phenyl-lower-alkyl-sulfinyl, alkylphenylsulfinyl, phenylsulfonyl, phenyl-lower-alkan-sulfonyl, or alkylphenylsulfonyl, whereas, if more than one rest Z is present (m≧2), the substituents Z are equal or different from each other, and wherein the bonds marked with an arrow are single or double bonds; or an N-oxide of said compound, wherein one ore more N-atoms carry an oxygene atom, or a salt thereof, and/or a compound of genaral formula IV

in which A has the meaning of group ═NR², W has the meaning of oxygen, sulfur, two hydrogen atoms or the group ═NR⁸, Z has the meaning of the group ═NR¹⁰ or ═N—, —N(R¹⁰)—(CH₂)_(q)-, branched or unbranched C₁₋₆-Alkyl or is the group

or A, Z and R¹ together form the group

m, n and o has the meaning of 0-3, q has the meaning of 1-6, R_(a), R_(b), R_(c), R_(d), R_(e), R_(f) independently from each other have the meaning of hydrogen, C₁₋₄ alkyl or the group ═NR¹⁰, and/or R_(a) and/or R_(b) together with R_(c) and or R_(d) or R_(c) together with R_(e) and/or R_(f) form a bound, or up to two of the groups R_(a)-R_(f) form a bridge with each up to 3 C-atoms with R¹ or R², X has the meaning of group ═NR⁹ or ═N—, Y has the meaning of group —(CH₂)_(p), p has the meaning of integer 1-4, R¹ has the meaning of unsubstituted or optionally substituted with one or more of halogene, C₁₋₆-alkyl, or C₁₋₆-alkyl or C₁₋₆alkoxy, which is optionally substituted by one or more of halogen, or is unsubstituted or substituted aryl or heteroaryl, R² has the meaning of hydrogen or C₁₋₆-alkyl, or form a bridge with up to 3 ring atoms with R_(a)-R_(f) together with Z or R₁, R³ has the meaning of monocyclic or bicyclic aryl or heteroaryl which is unsubstituted or optionally substituted with one or more of für halogen, C₁₋₆-alkyl, C₁₋₆-alkoxy or hydroxy, R⁴ ,R⁵, R⁶ and R⁷ independently from each other have the meaning of hydrogen, halogene or C₁₋₆-alkoxy, C₁₋₆-alkyl or C₁₋₆-carboxyalkyl, which are unsubstituted or optionally substituted with one or more of halogene, or R⁵ and R⁶ together form the group

R⁸, R⁹ and R¹⁰ independently from each other have the meaning of hydrogen or C₁₋₆-alkyl, as well as their isomers and salts, and/or a compound of general formula V

in which R¹ has the meaning of group

in which R⁵ is chloro, bromo or the group —OCH₃,

in which R⁷ is —CH₃ or chloro,

in which R⁸ is —CH₃, fluoro, in which R⁴ is fluoro, in which R⁶ is chloro or —CF₃ chloro, bromo, —CF₃, —CH₃ or chloro —N═C, —CH₃,—OCF₃ or —CH₂OH R² has the meaning of pyridyl or the group

and R³ has the meaning of hydrogen or fluoro, as well as their isomers and salts.
 16. Pharmaceutical compositions according to claim 15 which comprise as compound I and/or II (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate
 17. Pharmaceutical compositions according to claims 1-16 which comprise as compound I (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate, sTie2, mAB 4301-42-35, scFv-tTF and/or L19 scFv-tTF conjugate, and as compound II (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinatesTie2, mAB 4301-42-35, scFv-tTF and/or L19 scFv-tTF conjugate, with the provisio that compound I is not identically to compound II.
 18. Pharmaceutical compositions according to claims 1-17 which comprise as compound I (4-Chlorophenyl)[4-(4-pyridylmethyl)-phthalazin-1-yl]ammonium hydrogen succinate and as compound II sTie2, mAB 4301-42-35, scFv-tTF and/or L19 scFv-tTF conjugate.
 19. Pharmaceutical compositions according to claims 1-17 which comprise as compound I mAB 4301-42-35 and as compound II sTie2, and/or scFv-tTF conjugate.
 20. Pharmaceutical compositions according to claims 1-17 which comprise as compound I scFv-tTF conjugate and as compound II sTie2 and/or mAB 4301-42-35.
 21. Pharmaceutical compositions according to claims 1-17 which comprise as compound I L19 scFv-tTF conjugate and as compound II sTie2.
 22. Use of pharmaceutical compositions according to claims 1-21, for the production of a medicament for the treatment of tumors, cancers, psoriasis, arthritis, such as rheumatoide arthritis, hemangioma, angiofribroma, eye diseases, such as diabetic retinopathy, neovascular glaukoma, kidney diseases, such as glomerulonephritis, diabetic nephropathie, maligneous nephrosclerosis, thrombic microangiopatic syndrome, transplantation rejections and glomerulopathy, fibrotic diseases, such as cirrhotic liver, mesangial cell proliferative diseases, artheriosclerosis, damage of nerve tissues, suppression of the ascites formation in patients and suppression of VEGF oedemas. 